Novel plant monolignol synthesis, monolignol transport, and lignin polymerization genes and polypeptides encoded by such genes are provided. These genes and polynucleotide sequences are useful regulating the lignification process and plant phenotype. Moreover, these genes are useful for expression profiling of plant monolignol synthesis, monolignol transport, and lignin polymerization genes. The invention specifically provides polynucleotide and polypeptide sequences isolated from Eucalyptus and Pinus.
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1. An isolated polynucleotide comprising a nucleic acid sequence encoding seq id NO: 442 or a conservative variant of seq id NO: 442, wherein the conservative variant has a sequence identity that is greater than or equal to 95% to seq id NO: 442, and has the same functional properties of the polypeptide of seq id NO: 442.
3. The DNA construct of
4. The DNA construct of
6. The DNA construct of
7. The DNA construct of
8. A plant cell transformed with the DNA construct of
9. A transgenic plant comprising the plant cell of
10. The transgenic plant of
11. The transgenic plant of
12. The transgenic plant of
13. The transgenic plant of
14. Wood obtained from a transgenic tree which has been transformed with the DNA construct of
16. The isolated polynucleotide of
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I. Field of the Invention
The invention relates generally to the field of plant monolignol synthesis, monolignol transport, and lignin polymerization genes and polypeptides encoded by such genes, and the use of such polynucleotide and polypeptide sequences for controlling plant phenotype. The invention specifically provides polynucleotide and polypeptide sequences isolated from Eucalyptus and Pinus species and sequences related thereto.
II. Description of the Related Art
Lignin, a highly hydrophobic and crosslinked phenolic polymer, is a major component of the xylem of plants, especially woody plants such as angiosperm and gymnosperm trees. Lignin is composed of phenylpropanoid units derived from three cinnamyl alcohols, p-coumaroyl, coniferyl and sinapyl alcohol (each differing in the degree of methoxylation at the C3 and C5 positions of the aromic ring), although other phenolics can be incorporated. See, e.g., Sederoff et al. (1999) Curr. Opin. Plant Biol. 2:145-52. These alcohols are also known as monolignols.
Lignin is deposited within the cellulose framework of plant cell secondary cell walls by intussusception. The amount of ligninification varies among plant groups and species, cells and even between different parts of the same plant cell. See, e.g., T. T. Kozlowski and S. G. Pallardy (eds.), 1997, Physiology of Woody Plants, Academic Press, San Diego, Calif. For example, gymnosperm tracheids and angiosperm vessels are heavily lignified; whereas fiber tracheids and libriform fibers of angiosperms show little deposition of lignin. Besides its role as a structural component, lignin facilitates water transport, impedes the degradation of cell wall polysaccharides, and protects against disease-causing organisms, insects and other herbivores.
In contrast, lignin inhibits commercial exploitation of plants by impacting the structural properties of wood and wood products, as well as, the nutritional quality and digestibility of plants. Heavily lignified wood can significantly increase the cost of preparing fiber and wood products. For example, in order to make may grades of paper, it is necessary to remove much of the lignin content from the fiber network of wood. The removal of lignin during the pulping process is expensive, consumes large quantities of chemicals and energy, and potentially environmentally hazardous. Moreover, the difficulty of lignin extraction is relative to the complexity and heterogeneity of the polymer—lignin from gymnosperms, consisting mainly of guaiacyl subunits, is realatively more difficult to extract using Kraft delignification than lignin from angiosperms, consisting of both guaiacyl and syringyl subunits.
Likewise, heavily lignified plants are of poor nutritional quality as such plants generally have low levels of digestibility. As lignin is intimately associated with the cell wall polysaccharides of forages, it interferes with the digestion of those carbohydrates and hemicellulose by limiting their availability to enzymes.
The modulation of lignin content in plants by genetic engineering is an extremely powerful technique by which to ameliorate these negative plant qualities. See, e.g., Dean et al. (1997) Adv. Biochem. Eng. Biotechnol. 57:1-44. The control of lignin synthesis has applications such as the alteration of wood properties and, in particular, lumber and wood pulp properties. For example, wood pulp quality can be effected by increasing or decreasing the quantity or quality of lignin, cellulose, and nonlignin cell wall phenolics. Modulating lignin synthesis in a plant can also engineer functionally tailored lumber having increased or decreased dimensional stability, tensile strength, shear strength, compression strength, stiffness, hardness, spirility, shrinkage, weight, density and specific gravity.
A. The Lignification Process
The lignification process encompasses the biosynthesis of monolignols, their transport to the cell wall, and their polymerization into lignin. The lignification process has been extensively researched. However, new investigations have prompted commentators to note “that the traditional scheme of the lignin pathway is wrong in some respects.” Baucher et al., Crit. Rev. Biochem. Mol. Biol. 38(4):305-50 (2003). Importantly, skilled artisans recognize both their “limited understanding of the chemistry and biochemistry of the plant cell walls” and their ability to predict how specific genetic modifications will influence the ligninfication process. Baucher et al., supra.
Monolignol synthesis, i.e., that of p-coumaroyl, coniferyl and sinapyl alcohols, occurs through a complex series of reactions beginning with the amino acid phenylalanine and catalyzed by a number of multifunctional enzymes. See, e.g., Boerjan et al. (2003) Ann. Rev. Plant Biol. 54:519-46. In brief, the lignification process begins with the deamination of phenylalanine to form cinnamic acid. Cinnamic acid is modified by hydroxylation of the ring, subsequent methoxylation, and reduction of the modified cinnamic acids to cinnamyl alcohols, the monolignol precursors for lignin.
Specifically, the proteins cinnamyl alcohol dehydrogenase (CAD), caffeoyl-CoA O-methyl-transferase (CCoAOMT), cinnamoyl-CoA reductase (CCR), cinnamic acid 4-hydroxylase (C4H), p-coumarate 3-hydroxylase (C3H), 4-coumarate:CoA ligase (4CL), caffeic acid/5-hydroxyferulic acid O-methyltransferase (COMT), ferulate 5-hydroxylase (F5H), hydroxycinnamoyl-CoA:shikimate/quinate (HCT), laccase (LAC), phenylalanine ammonia-lyase (PAL), peroxidase (POX), and sinapyl alcohol dehydrogenase (SAD), each catalyze a reaction in the lignification process. See Humphreys J. M. and C. Chapple, Curr. Opin. Plant Biol. 5(3):224-229 (2002).
In addition to enzymes responsible for monolignol and lignin synthesis, specific enzymes assist in the export of lignin precursors from the cell cytoplasm to the secondary cell wall. Monolignols and monolignol precursors are subsequently chemically modified to assist in transportation and storage, by an array of cellular enzymes. See, e.g., Hosokawa et al., Plant Cell Physiol. 42(9):959-68 (2001). For example, the enzymes coniferol glucosyl transferase (CGT) and beta-glucosidase (CBG) may assist in exportation of coniferyl alcohol and coniferin.
Likewise, following the exportation process, enzymes are needed to catalyze the final steps of the polymerization process. The formation of the lignin macromolecule results from the oxidative coupling between a monolignol and the growing lignin polymer. See, e.g., R. Hatfield and W. Vermerris (2001) Plant Physiol. 126:1351-57. The enzymes phenolase (PNL), peroxidase (POX), laccase (LAC also known as multicopper oxidase) and other phenol oxydases catalyze the polymerization of monolignils into lignin.
Despite the degree of knowledge of the lignification process, significant uncertainties remain. For example, little is known of the storage of monolignols before they are transported to the cell wall. Similarly, skilled artisans generally do not know the subcellular localizations of most enzymes which catalyze lignification. Moreover, as discussed above, revisions of the lignification process have recently occurred as the result of new invesitigations into enzyme substate specificity and kinetics. Accordingly, new techniques are needed to investigate the role of specific enzymes in the lignification process.
B. Genetic Engineering of Plant Lignin Content
Previously, researchers have attempted to modulate the lignin content through the construction of transgenic plants. See, e.g., Baucher et al., supra. Although this research confirmed some of the recent revisions of the lignification process, it “has also opened up new research areas” and “posed new questions” for lignin research.
1. Up- and Down-Regulation of PAL
PAL catalyzes the non-oxidative deamination of phenylalanine to cinnamic acid. As this is the first step of the phenylpropanoid pathway, the reduction of PAL activity leads to a wide variety of abnormal phenotypes. See Elkind et al., Proc. Natl. Acad. Sci. U.S.A. 87:9057-9061 (1990). Transgenic tobacco plants were stunted, had abnormal leaves, reduced lignin content, and high incidence of fungal infection than wild-type plants. See Elkind et al., supra; Maher et al., Proc. Natl. Acad. Sci. U.S.A. 91:7802-7806 (1994).
2. Up- and Down-Regulation of C4H
Hydroxylation of cinnamic acid is catylzyed by C4H, a cytochrome P450-linked monooxygenase. In transgenic tobacco plants, overexpression of C4H had no effect on lignin content nor composition. See Sewalt et al., Plant Physiol. 115:41-50 (1997). In contrast, down-regulation of C4H led to decrease lignin content and altered lignin composition. See Sewalt et al., supra.
3. Down-Regulation of OMT
Transgenic plants which down-regulate OMT have been produced. See Zhong et al., Plant Physiol. 124:536-577 (2000). These plants demonstrated decreased lignin content primarily due to the reduction of both guaiacyl and syringyl subunits. Additionally, although the transgenic poplar were not affected in either growth or morphology, its lignin was much less cross-linked that wild-type poplar.
4. Up- and Down-Regulation of F5H
F5H was renamed coniferaldehyde 5-hydroxylase (Cald5H) upon the realization that it preferentially catalyzes the 5-hydroxylation of the cinnammaldehydes. See Baucher et al., supra. An Arabidopis mutant deficient in F5H reportedly produced lignin deficient in syringyl subunits. See Chapple et al., Plant Cell 4:1413-1424 (1992). Likewise, overexpression of a heterologous isoform of F5H in aspen produced an altered lignin compostition but failed to impact lignin content.
5. Down-Regulation of 4CL
Transgenic plants with reduced 4CL activity have been produced in aspen. See Hu et al., Nature Biotechnol. 17:808-812 (1999). Although these transgenic plants had decreased lignin content, normal cellular morphology and an increased growth rate, the apsens did not show any difference in the lignin composition. Additionally, the transgenic aspens possessed an increase in the amount of nonlignin cell wall phenolics.
6. Down-Regulation of CCR
CCR catalyzes a potential control point in the lignification process, namely the reduction of hydroxycinnamoyl-CoA thioesters to the corresponding aldehydes. Trangenic tobacco plants with down-regulated CCR activity demonstrated reduced lignin content and abnormal phenotypes, such as collapsed vessels, stunted growth, and abnormal leaf development. See, e.g., Goujon et al., Planta 217:218-228 (2003).
7. Down-Regulation of CAD
CAD catalyzes the final step of monolignal synthesis, i.e., the reduction of cinnamaldehydes to cinnamyl alcohols, and cad mutant plants and genetically-modified plants have been studied. An unusal cad mutant pine possessed an altered lignin composition, even to the extent of incorporating an unusual phenolic monomer. See Ralph et al., Science 277:235-239 (1997). Although the lignin of plants with low CAD activity is more extractable in alkali (see, e.g., Halpin et al., Plant J. 6:339-350 (1994)), lignin content is only slightly effected by the down-regulation of CAD activity (see Pilate et al., Nature Biotechnol. 20:607-612 (2002)).
8. Up- and Down-Regulation of Peroxidases
Peroxidases are believed to catalize the polymerization of lignin, yet no definitive proof have been presented for the involvement of any specific isozyme in vivo. See Baucher et al., supra. This is mainly due to both the large number of genes which encode peroxidases and the low substrate specificity of peroxidases. Although no change in lignin content and composition was observed in transgenic tobacco plants deficient in a major anionic peroxidase (see Lagrimini et al., Plant Physiol. 114:1187-1196 (1997)), a transgenic poplar with reduced anionic peroxidase activity demonstrated some reduced lignin content and altered lignin composition (see Yahong et al., In Molecular Breeding of Woody Plants (Progress in Biotechnology Series, Vol. 18), Elsevier Science, Amsterdam (2001)). Likewise, overexpression of peroxidase genes in poplar produced poor results, with no effect on overall plant phenotype or lignin content. See, e.g., Christensen et al., Plant Mol. Biol. 47:581-593 (2001).
9. Down-Regulation of Laccases
The role of laccases in the lignification process is still very much unclear. It is believed laccases participate in lignin polymerization. See, e.g., McDougall et al., Planta 194:9-14 (1994). However, transgenic Liriodendron (see Dean et al., In Lignin and Lignan Biosynthesis (ACS Symposium Series, Vol. 697), American Chemical Society, Washington, D.C.) and poplar (see Ranocha et al., Plant Physiol. 129:145-155 (2002)) down-regulating laccase had no altered phenotype nor any change in lignin content or composition.
As described above, many different transgenic plants are now available with altered lignin content, altered lignin composition or structure, or both. However, these experiments have few identified transgenic plants with distinct advantages in industrial operations, such as commercial pulping and papermaking. Additionally, these widely-divergent experimental results demonstrate the uncertainty apparent in the attempted modulation of the lignification process in transgenic plants.
C. Expression Profiling and Microarray Analysis of Monolignol Synthesis, Monolignol Transport, and Lignin Polymerization
The multigenic control of the lignification process presents difficulties in determining the genes responsible for phenotypic determination. One major obstacle to identifying genes and gene expression differences that contribute to phenotype in plants is the difficulty with which the expression of more than a handful of genes can be studied concurrently. Another difficulty in identifying and understanding gene expression and the interrelationship of the genes that contribute to plant phenotype is the high degree of sensitivity to environmental factors that plants demonstrate.
There have been recent advances using genome-wide expression profiling. In particular, the use of DNA microarrays has been useful to examine the expression of a large number of genes in a single experiment. Several studies of plant gene responses to developmental and environmental stimuli have been conducted using expression profiling. For example, microarray analysis was employed to study gene expression during fruit ripening in strawberry, Aharoni et al., Plant Physiol. 129:1019-1031 (2002), wound response in Arabodopsis, Cheong et al., Plant Physiol. 129:661-7 (2002), pathogen response in Arabodopsis, Schenk et al., Proc. Nat'l Acad. Sci. 97:11655-60 (2000), and auxin response in soybean, Thibaud-Nissen et al., Plant Physiol. 132:118. Whetten et al., Plant Mol. Biol. 47:275-91 (2001) discloses expression profiling of cell wall biosynthetic genes in Pinus taeda L. using cDNA probes. Whetten et al. examined genes which were differentially expressed between differentiating juvenile and mature secondary xylem. Additionally, to determine the effect of certain environmental stimuli on gene expression, gene expression in compression wood was compared to normal wood. 156 of the 2300 elements examined showed differential expression. Whetten, supra at 285. Comparison of juvenile wood to mature wood showed 188 elements as differentially expressed. Id. at 286.
Although expression profiling and, in particular, DNA microarrays provide a convenient tool for genome-wide expression analysis, their use has been limited to organisms for which the complete genome sequence or a large cDNA collection is available. See Hertzberg et al., Proc. Nat'l Acad. Sci. 98:14732-7 (2001a), Hertzberg et al., Plant J., 25:585 (2001b). For example, Whetten, supra, states, “A more complete analysis of this interesting question awaits the completion of a larger set of both pine and poplar ESTs.” Whetten et al. at 286. Furthermore, microarrays comprising cDNA or EST probes may not be able to distinguish genes of the same family because of sequence similarities among the genes. That is, cDNAs or ESTs, when used as microarray probes, may bind to more than one gene of the same family.
Methods of manipulating gene expression to yield a plant with a more desirable phenotype would be facilitated by a better understanding of monolignol synthesis, monolignol transport, and lignin polymerization gene expression in various types of plant tissue, at different stages of plant development, and upon stimulation by different environmental cues. The ability to control plant architecture and agronomically important traits would be improved by a better understanding of how monolignol synthesis, monolignol transport, and lignin polymerization gene expression effects formation of plant tissues and how plant growth and the lignification process are connected. Among the large number of genes, the expression of which can change during development of a plant, only a fraction are likely to effect phenotypic changes during any given stage of the plant development.
In one embodiment, DNA constructs useful for modulating the expression of monolignol synthesis, monolignol transport, and lignin polymerization are provided. In another embodiment, methods of modulating the expression lignin in plants are provided. In another embodiment, methods of making wood and wood pulp are provided. In addition, plant cells and plants that comprise DNA constructs useful for modulating the expression monolignol synthesis, monolignol transport, and lignin polymerization are provided.
In one embodiment, a polynucleotide comprises any one of the sequences of SEQ ID NOs: 1-252, 765 and 768, and conservative variants thereof. In one embodiment, the polynucleotide has a sequence identical to a gene sequence expressed in either Eucalyptus or Pinus species. In another embodiment, the convservative variant has a sequence identity that is greater than or equal to 99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%, 91%, 90%, 89%, 88%, 87%, 86%, 85%, 84%, 83%, 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75%, 74%, 73%, 72%, 71%, 70%, 69%, 68%, 67%, 66%, 65%, 64%, 63%, 62%, 61%, 60%, to any one of SEQ ID NOs: 1-252, 756 and 768. In another embodiment, such a conservative variant would further encode a protein possessing the activity of the protein of any one of SEQ ID NOs: 1-252, 756 and 768.
In another emobiment, a DNA construct comprises at least one of the polynucleotides of SEQ ID NOs: 1-252, 765 and 768. In yet another embodiment, a DNA construct comprises at least one of the polynucleotides of SEQ ID NOs: 1-252, 765 and 768, and an operably-linked promoter. In another embodiment, the DNA construct further comprises an operably-linked intron.
In one embodiment, the promoter can be a constitutive promoter, a strong promoter, an inducible promoter, a regulatable promoter, a temporally regulated promoter, and a preferred promoter. In another embodiment, the promoter can more specifically be an arabinogalactan gene family promoter, cinnamate 4-hydroxylase gene family promoter, nopaline synthase promoter, octopine synthase promoter, O-Methyltransferase gene family promoter, LIM protein gene family promoter, superubiquitin gene family promoter, and ubiquitin gene family promoter, and promoters for isozymes thereof. In yet another embodiment, the promoter can be the Arabidopsis ubiquitin 3 promoter, Arabidopsis ubiquitin 10 promoter, Arabidopsis ubiquitin 11 promoter, cauliflower mosaic virus 35S promoter, Eucalyptus Arabinogalactan promoter, Eucalyptus caffeic acid o-methyltransferase promoter, Pinus 4-coumarate CoA ligase promoter, Pinus cinnamate 4-hydroxylase promoter, Pinus LIM protein promoter, and Pinus superubiquitin promoter.
In one embodiment, the intron can be selected from a Eucalyptus xylem intron, PDK intron, superubiquitin intron, and YABBY intron.
In another embodiment, the polynucleotide encodes an RNA transcript. In one embodiment, the polynucleotide is in a sense or antisense orientation relative to the promoter. In yet another embodiment, the RNA transcript induces RNA interference of a polynucleotide having a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768.
In one embodiment, a plant cell transformed with DNA constructs is provided. In another embodiment, a transgenic plant comprising the transformed plant cell are provided. In one embodiment, the transformed plant is a woody plant. In another embodiment, the transformed plant is a tree. In yet another embodiment, the transformed plant is of a species of Eucalyptus or Pinus. In one embodiment, the plant may exhibit one or more traits, such as increased drought tolerance, herbicide resistance, reduced or increased height, reduced or increased branching, enhanced cold and frost tolerance, improved vigor, enhanced or altered color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced resistance of the wood to decay, enhanced resistance to fungal diseases, altered attractiveness to insect pests, increased disease tolerance, increased insect tolerance, increased water-stress'tolerance, improved texture, increased germination, increased micronutrient uptake, production of novel resins, and production of novel proteins or peptides, as compared to a plant of the same species that has not been transformed with the DNA construct. In another embodiment, the plant may exhibit one or more traits, such as a reduced period of juvenility, an increased period of juvenility, propensity to form reaction wood, self-abscising branches, accelerated reproductive development or delayed reproductive development, as compared to a plant of the same species that has not been transformed with the DNA construct.
In one embodiment, methods of making a transformed plant are provided. In another embodiment, methods of making a transformed plant are provided in which a phenotype of the transformed plant is different from a phenotype of a plant of the same species that has not been transformed with the DNA construct. In one embodiment, the phenotype of the transformed plant is lignin content, lignin composition, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization, fiber dimensions, lumen size, proportion of rays, proportion of vessel elements, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, accumulation of nonlignin cell wall phenolics, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape. In another embodiment, the phenotype that is different is increased or decreased relative percentage of the p-hydroxyphenyl subunit, increased or decreased relative percentage of the guaiacyl subunit, increased or decreased relative percentage of the sinapyl subunit, and an increased or decreased syringyl-to-guaiacyl ratio. In another embodiment, the phenotype that is different is the production and incorporation of syringyl monomer in lignin, and wherein the wild-type plant is characterized by lignin with little to no syringyl monomers.
In one embodiment, there is provided an isolated polynucleotide comprising a sequence encoding the catalytic or substrate-binding domain of a polypeptide of any one of SEQ ID NOs: 253-504, 766 and 769, in which the polynucleotide encodes a polypeptide having the activity of effecting monolignol synthesis, monolignol transport, or lignin polymerization. In another embodiment, an isolated polynucleotide is provided which comprises a sequence encoding the catalytic or substrate-binding domain of a polypeptide of any one of SEQ ID NOs: 253-504, 766 and 769, in which the polynucleotide encodes a polypeptide having the activity of the polypeptide of SEQ ID NOs: 253-504, 766 and 769.
In one embodiment, methods of making a transformed plant are provided comprising transforming a plant cell with a DNA construct having at least one polynucleotide of SEQ ID NOs: 1-252, 765 and 768, and their conservative variants, and culturing the transformed plant cell under conditions that promote growth of a plant. In another embodiment, the DNA construct transforming the plant cell comprises a promoter operably-linked to the polynucleotide. In another embodiment, the DNA construct transforming the plant cell further comprises an intron, and in which the promoter, polynucleotide, and intron are operably-linked. In another embodiment, the DNA construct transforming the plant cell comprises a polynucleotide encoding a polypeptide having an activity effecting monolignol synthesis, monolignol transport or lignin polymerization. In another embodiment, the DNA construct transforming the plant cell comprises a polynucleotide encoding a polypeptide having at least one activity, such as caffeate O-methyltransferase, caffeoyl-CoA O-methyltransferase, cinnamoyl-CoA reductase, trans-cinnamate 4-monooxygenase, coniferyl-alcohol glucosyltransferase, coniferin beta-glucosidase, coniferyl alcohol dehydrogenase, para-coumarate 3-monooxygenase, 4-coumarate CoA ligase, ferrulate 5-monooxygenase, laccase, mannitol dehydrogenase, peroxidase, and phenylalanine ammonia-lyase. In one embodiment, the methods comprise plant cells located within plant explant tissue.
In one embodiment, methods of making a transformed plant are provided, in which the phenotype is different in the transformed plant, as compared to a wild-type plant of the same species, when comparing, for instance, lignin content, lignin composition, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization, fiber dimensions, lumen size, proportion of rays, proportion of vessel elements, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, accumulation of nonlignin cell wall phenolics, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape. In another embodiment, a phenotype that is different in the transformed plant, as compared to a wild-type plant of the same species, is a lignin modification such as increased or decreased relative percentage of the p-hydroxyphenyl subunit, increased or decreased relative percentage of the guaiacyl subunit, increased or decreased relative percentage of the sinapyl subunit, and an increased or decreased syringyl-to-guaiacyl ratio. In another embodiment, the phenotype that is different in the transformed plant, as compared to a wild-type plant of the same species, is the production and incorporation of syringyl monomer in lignin, and in which the wild-type plant is characterized by lignin incorporating little to no syringyl monomers.
In one embodiment, methods of making a transformed plant are provided in which a phenotype that is different in the transformed plant, as compared to a wild-type plant of the same species, is modified by increased drought tolerance, herbicide resistance, reduced or increased height, reduced or increased branching, enhanced cold and frost tolerance, improved vigor, enhanced or altered color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced resistance of the wood to decay, enhanced resistance to fungal diseases, altered attractiveness to insect pests, increased disease tolerance, increased insect tolerance, increased water-stress tolerance, improved texture, increased germination, increased micronutrient uptake, production of novel resins, and production of novel proteins or peptides, as compared to a plant of the same species that has not been transformed with the DNA construct. In another embodiment, the phenotype that is different in the transformed plant, as compared to a wild-type plant of the same species, is modified by a reduced period of juvenility, an increased period of juvenility, propensity to form reaction wood, self-abscising branches, accelerated reproductive development or delayed reproductive development, as compared to a plant of the same species that has not been transformed with the DNA construct.
In one embodiment, wood is provided which has been obtained from a transgenic tree which has been transformed by an inventive DNA construct. In another embodiment, the wood comprises an altered, as compared to wood obtained from a wild-type plant of the same species, trait such as lignin content, lignin composition, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization, fiber dimensions, lumen size, proportion of rays, proportion of vessel elements, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, accumulation of nonlignin cell wall phenolics, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape. In another embodiment, the wood comprises an altered trait such as increased or decreased relative percentage of the p-hydroxyphenyl subunit, increased or decreased relative percentage of the guaiacyl subunit, increased or decreased relative percentage of the sinapyl subunit, and an increased or decreased syringyl-to-guaiacyl ratio. In another embodiment, the wood comprises lignin of an altered S/G ratio, as compared to wood from a wild-type plant, such as an increased S/G ratio and a decreased S/G ratio. In another embodiment, the wood degrades faster than that of wood from a wild-type plant or more efficiently undergoes delignification than wood from a wild-type plant. In another embodiment, the wood comprises lignin possessing the syringyl subunit but in which the wild-type plant is characterized by lignin with little to no syringyl monomers.
In one embodiment, methods of making wood are provided comprising transforming a plant with a DNA construct comprising a polynucleotide having a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768, and conservative variants thereof, culturing the transformed plant under conditions that promote growth of a plant; and obtaining wood from the plant.
In another embodiment, wood pulp is provided which has been obainted from a transgenic tree transformed with the inventive DNA constructs.
In one embodiment, methods of making wood pulp are provided comprising transforming a plant with an inventive DNA construct; culturing the transformed plant under conditions that promote growth of a plant; and obtaining wood pulp from the plant. In another embodiment, the wood pulp is obtained from the plant by any pulping process, such as mechanical pulping, thermomechanical pulping, enzymatic pulping, chemical pulping, or chemithermomechanical pulping. In another embodiment, chemical pulping processing can consist of acidic or bisulfate pulping, sulfate pulping, Kraft pulping, soda pulping, anthraquinone pulping, or Kraft-anthraquinone pulping.
In one embodiment, polypeptide comprising an amino acid sequence encoded by the inventive isolated polynucleotides are provided. In another embodiment, isolated polypeptides are provided comprising amino acid sequences such as SEQ ID NOs: 253-504, 766 and 769.
In another embodiment, methods of altering a phenotype of a plant are provided comprising altering expression in the plant of a polypeptide encoded by any one of SEQ ID NOs: 253-504, 766 and 769. In another embodiment, the expression in a plant can be up-regulated, down-regulated, silenced, or developmentally-regulated. In another embodiment, the method of altering expression takes place in a woody plant. In another embodiment, the altered plant phenotype is a trait such as lignin content, lignin composition, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization, fiber dimensions, lumen size, proportion of rays, proportion of vessel elements, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, accumulation of nonlignin cell wall phenolics, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape. In another embodiment, the plant exhibits one or more traits such as increased drought tolerance, herbicide resistance, reduced or increased height, reduced or increased branching, enhanced cold and frost tolerance, improved vigor, enhanced color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced resistance of the wood to decay, enhanced resistance to fungal diseases, altered attractiveness to insect pests, increased disease tolerance, increased insect tolerance, increased water-stress tolerance, improved texture, increased germination, increased micronutrient uptake, production of novel resins, increased cellulose content, decreased lignin content and production of novel proteins or peptides, as compared to a plant of the same species that has not been transformed with the DNA construct.
In one embodiment, methods of altering a phenotype of a plant are provided in which the plant possesses lignin having one or more traits such as increased or decreased relative percentage of the p-hydroxyphenyl subunit, increased or decreased relative percentage of the guaiacyl subunit, increased or decreased relative percentage of the sinapyl subunit, and an increased or decreased syringyl-to-guaiacyl ratio. In another embodiment, the lignin has an altered S/G ratio, as compared to wood from a wild-type plant, such as an increased S/G ratio and a decreased S/G ratio.
In one embodiment, a polynucleotide is provided comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 505-756, 767 and 770.
In another aspect, the present invention provides method of correlating gene expression in two different samples, comprising detecting a level of expression of one or more genes encoding a product encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768 and conservative variants thereof in a first sample, detecting a level of expression of the one or more genes in a second sample, comparing the level of expression of the one or more genes in the first sample to the level of expression of the one or more genes in the second sample, and correlating a difference in expression level of the one or more genes between the first and second samples.
In a further aspect, the present invention provides a method of correlating the possession of a plant phenotype to the level of gene expression in the plant of one or more genes comprising detecting a level of expression of one or more genes encoding a product encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768 and conservative variants thereof in a first plant possessing a phenotype, detecting a level of expression of the one or more genes in a second plant lacking the phenotype, comparing the level of expression of the one or more genes in the first plant to the level of expression of the one or more genes in the second plant, and correlating a difference in expression level of the one or more genes between the first and second plants to possession of the phenotype.
In an additional aspect, the invention provides a method of correlating gene expression to propensity to form reaction wood, comprising detecting a level of expression of one or more genes encoding a product encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768 and conservative variants thereof in a first plant cell in xylem displaying a normal wood phenotype, detecting a level of expression of the one or more genes in a second plant cell in xylem displaying a reaction wood phenotype, comparing the level of the expression of the one or more genes in the first plant cells to the level of expression of the one or more genes in the second plants cells, and correlating a difference in expression level of the one or more genes between the first and second samples to the propensity to form reaction wood.
In one aspect, the present invention provides a combination for detecting expression of one or more genes, comprising two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768.
In another aspect, the present invention provides a combination for detecting expression of one or more genes, comprising two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to gene product encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768.
In a further aspect, the present invention provides a microarray comprising a combination of the present invention on a solid support, wherein each of said two or more oligonucleotides occupies a unique location on said solid support.
In an additional aspect, the present invention provides a method for detecting one or more genes in a sample, comprising contacting the sample with two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a gene comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768 under standard hybridization conditions and detecting the one or more genes of interest which are hybridized to the one or more oligonucleotides.
In one aspect, the present invention provides a method for detecting one or more nucleic acid sequences encoded by one or more genes in a sample, comprising contacting the sample with two or more oligonucleotides, wherein each oligonucleotide is capable of hybridizing to a nucleic acid sequence encoded by a gene comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-252, 765 and 768 under standard hybridization conditions and detecting the one or more nucleic acid sequences which are hybridized to the one or more oligonucleotides.
In one aspect, the present invention provides a kit for detecting gene expression comprising a microarray together with one or more buffers or reagents for a nucleotide hybridization reaction.
Other objects, features and advantages of the present invention will become apparent from the following detailed description. The detailed description and specific examples, while indicating preferred embodiments, are given for illustration only since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description. Further, the examples demonstrate the principle of the invention and cannot be expected to specifically illustrate the application of this invention to all the examples where it will be obviously useful to those skilled in the prior art.
The invention provides novel isolated lignin synthesis, transport and polymerization genes and polynucleotides useful for altering the phenotypic properties of plants. The invention also provides methods for identifying multigenic factors that contribute to a phenotype and for manipulating gene expression to affect plant phenotype. These genes were derived from plants of commercially important forestry genera, pine and eucalyptus. These genes are involved in each stage of the lignificiation process—monolignol synthesis, monolignol transport, and the final polymerization of lignin—and are, at least in part, responsible for the expression of phenotypic characteristics important in the commercial industry, including, but not limited to, cellulose and lignin content, coarseness, density, extratives content, fiber dimensions, stiffness, and strength. Generally, the genes and polynucleotides encode proteins which can be cinnamate-4-hydroxylase, cinnamoyl-CoA reductase, cinnamoyl alcohol dehydrogenase, 4-coumarate-CoA ligase, coumarate 3-hydroxylase, coniferin beta-glucosidase, coniferyl alcohol dehydrogenase, coniferyl aldehyde 5-hydrolase, cytocrome p450, dihydroflavonol 4-reductase, multicopper oxidase, o-methyltransferase, peroxidase, phenolase, phenylalanine ammonia lyase, sinapyl alcohol dehydrogenase, SPI2 protein, and UDP-glucosyltransferase.
The methods of the present invention for selecting and using lignin synthesis, transportation, and polymerization genes for modulation of lignin synthesis provide transgenic plants with more highly engineered phenotypes. The ability to control plant architecture and agronomically important traits in plants is improved.
Unless indicated otherwise, all technical and scientific terms are used herein in a manner that conforms to common technical usage. Generally, the nomenclature of this description and the described laboratory procedures, including cell culture, molecular genetics, and nucleic acid chemistry and hybridization, respectively, are well known and commonly employed in the art. Standard techniques are used for recombinant nucleic acid methods, oligonucleotide synthesis, cell culture, tissue culture, transformation, transfection, transduction, analytical chemistry, organic synthetic chemistry, chemical syntheses, chemical analysis, and pharmaceutical formulation and delivery. Generally, enzymatic reactions and purification and/or isolation steps are performed according to the manufacturers' specifications. Absent an indication to the contrary, the techniques and procedures in question are performed according to conventional methodology disclosed, for example, in Sambrook J. and D. W. Russell (2001) M
I. Monolignol Synthesis, Monolignol Transport, and Lignin Polymerization Genes, Polynucleotide and Polypeptide Sequences
One aspect of the present invention relates to novel monolignol synthesis, monolignol transport, and lignin polymerization genes and polypeptides encoded by such genes.
The present invention provides novel plant monolignol synthesis, monolignol transport, and lignin polymerization genes and polynucleotides and novel monolignol synthesis, monolignol transport, and lignin polymerization proteins and polypeptides. In one embodiment, the novel monolignol synthesis, monolignol transport, and lignin polymerization genes are the same as those expressed in a wild-type plant of a species of Pinus or Eucalyptus. As used herein, “wild-type” refers generally to a phenotype, genotype, or gene in a population or stain of organisms in contrast to that of organisms transformed by laboratory techniques. Specific exemplary novel plant monolignol synthesis, monolignol transport, and lignin polymerization gene sequences of the invention are set forth in TABLE 1, TABLE 2, TABLE 3, and TABLE 4, which comprise Pinus radiata gene sequences, corresponding protein sequences encoded by those genes, and related oligonucleotide sequences, and TABLE 5, TABLE 6, TABLE 7, and TABLE 8, which comprise Eucalyptus grandis gene sequences, corresponding protein sequences encoded by those genes, and related oligonucleotide sequences.
The sequences of the invention have monolignol synthesis, monolignol transport, and/or lignin polymerization activity and encode proteins that are active in monolignol synthesis, such as proteins of the cinnamic acid and sinapyl alcohol enzymatic pathways, monolignol transport, such as caffeate O-methyltransferase, caffeoyl-CoA O-methyltransferase, cinnamoyl-CoA reductase, trans-cinnamate 4-monooxygenase, coniferyl-alcohol glucosyltransferase, coniferin beta-glucosidase, coniferyl alcohol dehydrogenase, para-coumarate 3-monooxygenase, 4-coumarate CoA ligase, ferrulate 5-monooxygenase, laccase, mannitol dehydrogenase, peroxidase, and phenylalanine ammonia-lyase. As discussed below, manipulation of the expression of the monolignol synthesis, monolignol transport, and lignin polymerization genes and polynucleotides, or manipulation of the activity of the encoded proteins and polypeptides, can resulting a transgenic plant with a desired phenotype that differs from the phenotype of a wild-type plant of the same species.
The present invention also includes sequences that are complements, reverse sequences or reverse compliments to the nucleotide sequences disclosed herein.
Throughout this description, reference is made to monolignol synthesis, monolignol transport, and lignin polymerization genes products. As used herein, a “monolignol synthesis, monolignol transport, or lignin polymerization gene product” is a product encoded by a monolignol synthesis, monolignol transport, or lignin polymerization gene, including both nucleotide products, such as DNA and RNA, and amino acid products, such as proteins and polypeptides. Monolignol synthesis, monolignol transport, or lignin polymerization gene products possess enzamatic or catalytic activities useful in the biosynthesis of monolignols, the transport of monolingols, or the polymerization of lignin. Exemplary monolignol synthesis, monolignol transport, or lignin polymerization gene products include, but are not limited to, caffeate O-methyltransferase, caffeoyl-CoA O-methyltransferase, cinnamoyl-CoA reductase, trans-cinnamate 4-monooxygenase, coniferyl-alcohol glucosyltransferase, coniferin beta-glucosidase, coniferyl alcohol dehydrogenase, para-coumarate 3-monooxygenase, 4-coumarate CoA ligase, ferrulate 5-monooxygenase, laccase, mannitol dehydrogenase, peroxidase, and phenylalanine ammonia-lyase. Moreover, gene products possessing O-methyltransferase activity may possesses a specific substrated activity including, but not limited to, 5-hydroxyconiferyl aldehyde O-methyltransferase (AldOMT), caffeic acid O-methyltransferase, caffeoyl-CoA O-methyltransferase, catechol-CoA O-methyltransferase, and inositol O-methyltransferase. Likewise, gene products possessing peroxidase activity may possesses a specific substrated activity including, but not limited to, anionic peroxidase, ascorbate peroxidase, and cationic peroxidase.
Examples of specific monolignol synthesis, monolignol transport, and lignin polymerization genes include SEQ ID NOs: 1-252, 756 and 768. Examples of specific monolignol synthesis, monolignol transport, and lignin polymerization gene products of the invention include products encoded by any one of SEQ ID NOs: 1-252, 756 and 768. Examples of specific monolignol synthesis, monolignol transport, and lignin polymerization proteins and polypeptides of the invention include polypeptides encoded by any of SEQ ID NOs: 253-504, 766 and 769 or polypeptides comprising the amino acid sequence of any of SEQ ID NOs: 1-252, 756 and 768. Another aspect of the invention is directed to conservative variants, as defined below, of these specific monolignol synthesis, monolignol transport, and lignin polymerization genes and their nucleotide and amino acid products.
The present invention also includes conservative variants of the sequences disclosed herein. The term “variant” refers to a nucleotide or amino acid sequence that differs in one or more nucleotide bases or amino acid residues from the reference sequence of which it is a variant.
Accordingly, in one respect, the invention includes conservative variant polynucleotides. As used herein, the term “conservative variant polynucleotide” refers to a polynucleotide that hybridizes under stringent conditions to an oligonucleotide probe that, under comparable conditions, binds to the reference gene the conservative variant is a variant of. Thus, for example, a conservative variant of SEQ ID NO: 1 hybridizes under stringent conditions to an oligonucleotide probe that, under comparable conditions, binds to SEQ ID NO: 1. For example, sequences are considered to hybridize when they form a double-stranded complex in a hybridization solution of 6×SSC, 0.5% SDS, 5×Denhardt's solution and 100 μg of non-specific carrier DNA. See Ausubel et al., section 2.9, supplement 27 (1994). “Moderate stringency” is defined as a temperature of 60° C. in a hybridization solution of 6×SSC, 0.5% SDS, 5×Denhardt's solution and 100 μg of non-specific carrier DNA. Id. “High stringency” hybridization conditions are, for example, 68° C. in a hybridization solution of 6×SSC, 0.5% SDS, 5×Denhardt's solution and 100 μg of non-specific carrier DNA. Following the moderate stringency hybridization reaction, the nucleotides are washed in a solution of 2×SSC plus 0.05% SDS for five times at room temperature, with subsequent washes with 0.1×SSC plus 0.1% SDS at 60° C. for 1 h.
One aspect of the invention provides conservative variant polynucleotides that exhibit at least about 75% sequence identity to their respective reference sequences. “Sequence identity” has an art-recognized meaning and can be calculated using published techniques. See C
Methods to determine identity and similarity are codified in and executed by, for example, computer programs and algorithms. Preferred computer program methods to determine identity and similarity between two sequences include but are not limited to the GCG program package (Devereux et al., Nucleic Acids Research 12: 387 (1984)), BLASTP, BLASTN, FASTA (Atschul et al., J. Mol. Biol. 215: 403 (1990)), and FASTDB (Brutlag et al., Comp. App. Biosci. 6: 237 (1990)).
The invention includes conservative variant polynucleotides having a sequence identity that is greater than or equal to 99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%, 91%, 90%, 89%, 88%, 87%, 86%, 85%, 84%, 83%, 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75%, 74%, 73%, 72%, 71%, 70%, 69%, 68%, 67%, 66%, 65%, 64%, 63%, 62%, 61%, or 60% to any one of SEQ ID NO: 1-252, 756 and 768. In such variants, differences between the variant and the reference sequence can occur at the 5′ or 3′ terminal positions of the reference nucleotide sequence or anywhere between those terminal positions, interspersed either individually among nucleotides in the reference sequence or in one or more contiguous groups within the reference sequence.
Additional conservative variant polynucleotides contemplated by and encompassed within the present invention include polynucleotides comprising sequences that differ from the polynucleotide sequences of SEQ ID NOs: 1-252, 756 and 768 or complements, reverse complements or reverse sequences thereof, as a result of deletions and/or insertions totaling less than 30% of the total sequence length. In one embodiment, deletions and/or insertions total less than 20% or less than 10% of the total length.
The invention also includes conservative variant polynucleotides that, in addition to sharing a high degree of similarity in their primary structure (sequence) to SEQ ID NOs have at least one of the following features: (i) they contain an open reading frame or partial open reading frame encoding a polypeptide having substantially the same functional properties in polynucleotide synthesis as the polypeptide encoded by the reference polynucleotide, or (ii) they have nucleotide domains or encoded protein domains in common. The invention includes conservative variants of SEQ ID NOs: 1-252, 756 and 768 that encode proteins having the enzyme or biological activity or binding properties of the protein encoded by the reference polynucleotide. Such conservative variants are functional variants, in that they have the enzymatic or binding activity of the protein encoded by the reference polynucleotide.
In accordance with one embodiment, polynucleotide variants can include a “shuffled gene” such as those described in e.g. U.S. Pat. Nos. 6,500,639, 6,500,617, 6,436,675, 6,379,964, 6,352,859 6,335,198 6,326,204, and 6,287,862. A variant of a nucleotide sequence of the present invention also can be a polynucleotide modified as disclosed in U.S. Pat. No. 6,132,970, which is incorporated herein by reference.
In accordance with one embodiment, the invention provides a polynucleotide that encodes a monolignol synthesis, monolignol transport, and lignin polymerization protein such as beta-glucosidase, beta-mannasidase, cinnamate-4-hydroxylase, cinnamoyl-CoA reductase, cinnamoyl alcohol dehydrogenase, 4-coumarate-CoA ligase, coumarate 3-hydroxylase, coniferyl alcohol dehydrogenase, coniferyl aldehyde 5-hydrolase, cytocrome p450, dihydroflavonol 4-reductase, diphenol oxidase, multicopper oxidase, O-methyltransferase, peroxidase, phenolase, phenylalanine ammonia lyase, sinapyl alcohol dehydrogenase, SPI2 protein, and UDP-glucosyltransferase. Moreover, the O-methyltransferase protein may be any of 5-hydroxyconiferyl aldehyde O-methyltransferase (AldOMT), caffeic acid O-methyltransferase, caffeoyl-CoA O-methyltransferase, catechol-CoA O-methyltransferase, or inositol O-methyltransferase. Likewise, the peroxidase may be anionic peroxidase, ascorbate peroxidase, and cationic peroxidase. SEQ ID NOs: 1-252, 756 and 768 provide examples of such polynucleotides.
In accordance with another embodiment, a polynucleotide of the invention encodes the catalytic or protein binding domain of a polypeptide encoded by any of SEQ ID NOs: 1-252, 756 and 768 or of a polypeptide comprising any of SEQ ID NOs: 253-504, 766 and 769. The catalytic and protein binding domains of the monolignol synthesis, monolignol transport, and lignin polymerization proteins of the invention are known in the art. The conserved sequences of these proteins are shown in
The invention also includes conservative variant polynucleotides that differ from the sequences discussed above but that, as a consequence of the degeneracy of the genetic code, encode a polypeptide which is the same as that encoded by a polynucleotide of the present invention. The invention also includes as conservative variants polynucleotides comprising sequences that differ from the polynucleotide sequences discussed above as a result of substitutions that do not affect the amino acid sequence of the encoded polypeptide sequence, or that result in conservative substitutions in the encoded polypeptide sequence.
The present invention also includes an isolated polypeptide encoded by a polynucleotide comprising any of SEQ ID NOs: 1-252, 756 and 768 or any of the conservative variants thereof discussed above. The invention also includes polypeptides comprising SEQ ID NOs: 253-504, 766 and 769 and conservative variants of these polypeptides.
In accordance with the invention, a variant polypeptide or protein refers to an amino acid sequence that is altered by the addition, deletion or substitution of one or more amino acids.
The invention includes conservative variant polypeptides. As used herein, the term “conservative variant polypeptide” refers to a polypeptide that has similar structural, chemical or biological properties to the protein it is a conservative variant of. Guidance in determining which amino acid residues can be substituted, inserted, or deleted can be found using computer programs well known in the art such as Vector NTI Suite (InforMax, MD) software. In one embodiment of the invention, conservative variant polypeptides that exhibit at least about 75% sequence identity to their respective reference sequences.
Conservative variant protein includes an “isoform” or “analog” of the polypeptide. Polypeptide isoforms and analogs refers to proteins having the same physical and physiological properties and the same biological function, but whose amino acid sequences differs by one or more amino acids or whose sequence includes a non-natural amino acid.
Polypeptides comprising sequences that differ from the polypeptide sequences of SEQ ID NO: 253-504, 766 and 769 as a result of amino acid substitutions, insertions, and/or deletions totaling less than 10% of the total sequence length are contemplated by and encompassed within the present invention.
One aspect of the invention provides conservative variant polypeptides function in monolignol synthesis, monolignol transport, and/or lignin polymerization, as determined by one or more appropriate assays, such as those described below. The invention includes variant polypeptides which are monolignol synthesis, monolignol transport, and lignin polymerization proteins, such as those capable of conjugating p-courmarate and Co-enzyme A or those peptides having an O-methyltransferase biological activity. As discussed above, the invention includes variant polynucleotides which encode polypeptides that function as monolignol synthesis, monolignol transport and lignin polymerization proteins.
The activities and physical properties of monolignol synthesis, monolignol transport and lignin polymerization proteins can be examined using any method known in the art. The following examples of assay methods are not exhaustive and are included to provide some guidance in examining the activity and distinguishing protein characteristsics of monolignol synthesis, monolignol transport and lignin polymerization proteins variants.
Phenylalanine ammonia lyase (PAL), and other monolignol synthesis, monolignol transport and lignin polymerization, activity can be measured using a radiometric assay. Briefly, leaf and flower samples are collected and snap frozen in liquid nitrogen. PAL activity can then be measured in cell extracts by a radiometric assay as described in Dixon et al., Physiol. Plant Pathol. 13:295-306 (1978). Cinnamoyl alcohol dehydrogenase (CAD) assays can be carried out in 1 mL of 100 mM Tris-HCl pH 8.8, containing 50 to 100 μL of plant extract, 0.1 mM coniferyl alcohol, and 0.02 mM NADP and monitored at 400 nm over 15 min at 30° C. See, e.g., Abbott et al., Plant Physiol. 128(3):844-53 (2002). Caffeate/5-hydroxyferulate O-methyltransferase (COMT) can be assayed by the protocol of Fukuda H. and A. Komamine, Planta 155:423-430 (1982), with minor modifications. Cinnamoyl-coenzyme A reductase (CCR) assays (350 μL) can contain 100 mM KH2PO4-Na2HPO4, pH 6.25; 5 mM dithiothreitol; 100 μM NADPH; 30 μM 14 C feruloyl coenzyme A (13,000 dpm); and 30 μL of plant extract. See, e.g., Abbott et al., Plant Physiol. 128(3):844-53 (2002). Control reactions can be carried out by omitting NADPH. These assay reactions can be incubated at about 30° C. for about 10 min, stopped with about 1 mL of ethyl acetate, vortexed, and partitioned by centrifugation. About five hundred microliters of the organic phase can be counted in 4.5 mL of Ecoscint scintillator (National Diagnostics, Hull, Herts, UK).
II. Methods of Using Monolignol Synthesis, Monolignol Transport, and Lignin Polymerization Genes, Polynucleotide and Polypeptide Sequences
The present invention provides methods of using monolignol synthesis, monolignol transport, and lignin polymerization genes and conservative variants thereof. The invention includes methods and constructs for altering expression of monolignol synthesis, monolignol transport, and lignin polymerization, and monolignol synthesis, monolignol transport, and lignin polymerization-like genes and/or gene products for purposes including, but not limited to (i) investigating function during monolignol synthesis, monolignol transport, and lignin polymerization and ultimate effect on plant phenotype and (ii) to effect a change in plant phenotype. For example, the invention includes methods and tools for modifying wood quality, fiber development, secondary cell wall lignin content, and plant growth and yield by altering expression of one or more monolignol synthesis, monolignol transport, and lignin polymerization genes.
The invention comprises methods of altering the expression of any of the monolignol synthesis, monolignol transport, and lignin polymerization genes and variants discussed above. Thus, for example, the invention comprises altering expression of a monolignol synthesis, monolignol transport, or lignin polymerization gene present in the genome of a wild-type plant of a species of Eucalyptus or Pinus. In one embodiment, the monolignin synthesis, monolignol transport, or lignin polymerization gene comprises a nucleotide sequence selected from SEQ ID NOs: 1-252, 756 and 768 sequences or the conservative variants thereof, as discussed above.
A. Techniques to Alter Gene Expression
Techniques which can be employed in accordance with the present invention to alter gene expression, include, but are not limited to: (i) over-expressing a gene product, (ii) disrupting a gene's transcript, such as disrupting a gene's mRNA transcript; (iii) disrupting the function of a polypeptide encoded by a gene, or (iv) disrupting the gene itself. Over-expression of a gene product, the use of antisense RNAs, ribozymes, and the use of double-stranded RNA interference (dsRNAi) are valuable techniques for discovering the functional effects of a gene and for generating plants with a phenotype that is different from a wild-type plant of the same species.
Over-expression of a target gene often is accomplished by cloning the gene or cDNA into an expression vector and introducing the vector into recipient cells. Alternatively, over-expression can be accomplished by introducing exogenous promoters into cells to drive expression of genes residing in the genome. The effect of over-expression of a given gene on cell function, biochemical and/or physiological properties can then be evaluated by comparing plants transformed to over-express the gene to plants that have not been transformed to over-express the gene.
Antisense RNA technology involves expressing in, or introducing into, a cell an RNA molecule (or RNA derivative) that is complementary to, or antisense to, sequences found in a particular mRNA in a cell. The antisense RNA can inhibit translation of the encoded gene product. The use of antisense technology to reduce or inhibit the expression of specific plant genes has been described, for example in European Patent Publication No. 271988, Hu et al., Nature Biotechnol. 17:808-812 (1999); Sederoff, R. R., Nature Biotechnol: 17:750-751 (1999); Smith et al., Nature, 334:724-726 (1988); Smith et. al., Plant Mol. Biol., 14:369-379 (1990)).
A ribozyme is an RNA that has both a catalytic domain and a sequence that is complementary to a particular mRNA. The ribozyme functions by associating with the mRNA (through the complementary domain of the ribozyme) and then cleaving (degrading) the message using the catalytic domain. RNA interference (RNAi) involves a post-transcriptional gene silencing (PTGS) regulatory process, in which the steady-state level of a specific mRNA is reduced by sequence-specific degradation of the transcribed, usually fully processed mRNA without an alteration in the rate of de novo transcription of the target gene itself. The RNAi technique is discussed, for example, in Elibashir, et al., Methods Enzymol. 26: 199 (2002); McManus & Sharp, Nature Rev. Genetics 3: 737 (2002); PCT application WO 01/75164; Martinez et al., Cell 110: 563 (2002); Elbashir et al., supra; Lagos-Quintana et al., Curr. Biol. 12: 735 (2002); Tuschl et al., Nature Biotechnol. 20:446 (2002); Tuschl, Chembiochem. 2: 239 (2001); Harborth et al., J. Cell Sci. 114: 4557 (2001); et al., EMBO J. 20:6877 (2001); Lagos-Quintana et al., Science. 294: 8538 (2001); Hutvagner et al., loc cit, 834; Elbashir et al., Nature. 411: 494 (2001).
B. Assembly of DNA Constructs
The present invention provides a DNA construct comprising at least one polynucleotide of SEQ ID NOs: 1-252, 756 and 768 or conservative variants thereof, such as the conservative variants discussed above. Any method known in the art can be used to generate the DNA constructs of the present invention. See, e.g. Sambrook et al., supra.
The invention includes DNA constructs that optionally comprise a promoter. Any suitable promoter known in the art can be used. A promoter is a nucleic acid, preferably DNA, that binds RNA polymerase and/or other transcription regulatory elements. As with any promoter, the promoters of the invention facilitate or control the transcription of DNA or RNA to generate an mRNA molecule from a nucleic acid molecule that is operably linked to the promoter. The RNA can encode a protein or polypeptide or can encode an antisense RNA molecule or a molecule useful in RNAi. Promoters useful in the invention include constitutive promoters, inducible promoters, temporally regulated promoters and tissue-preferred promoters.
Examples of useful constitutive plant promoters include: the cauliflower mosaic virus (CaMV) 35S promoter, which confers constitutive, high-level expression in most plant tissues (Odel et al. Nature 313:810 (1985)); the nopaline synthase promoter (An et al. Plant Physiol. 88:547 (1988)); and the octopine synthase promoter (Fromm et al., Plant Cell 1: 977 (1989)). It should be noted that, although the CaMV 35S promoter is commonly referred to as a constitutive promoter, some tissue preference can be seen. The use of CaMV 35S is envisioned by the present invention, regardless of any tissue preference which may be exhibited during use in the present invention.
Inducible promoters regulate gene expression in response to environmental, hormonal, or chemical signals. Examples of hormone inducible promoters include auxin-inducible promoters (Baumann et al. Plant Cell 11:323-334 (1999)), cytokinin-inducible promoters (Guevara-Garcia, Plant Mol. Biol. 38:743-753 (1998)), and gibberellin-responsive promoters (Shi et al. Plant Mol. Biol. 38:1053-1060 (1998)). Additionally, promoters responsive to heat, light, wounding, pathogen resistance, and chemicals such as methyl jasmonate or salicylic acid, can be used in the DNA constructs and methods of the present invention.
Tissue-preferred promoters allow for preferred expression of polynucleotides of the invention in certain plant tissue. Tissue-preferred promoters are also useful for directing the expression of antisense RNA or siRNA in certain plant tissues, which can be useful for inhibiting or completely blocking the expression of targeted genes as discussed above. As used herein, vascular plant tissue refers to xylem, phloem or vascular cambium tissue. Other preferred tissue includes apical meristem, root, seed, and flower. In one aspect, the tissue-preferred promoters of the invention are either “xylem-preferred,” “cambium-preferred” or “phloem-preferred,” and preferentially direct expression of an operably linked nucleic acid sequence in the xylem, cambium or phloem, respectively. In another aspect, the DNA constructs of the invention comprise promoters that are tissue-specific for xylem, cambium or phloem, wherein the promoters are only active in the xylem, cambium or phloem.
A vascular-preferred promoter is preferentially active in any of the xylem, phloem or cambium tissues, or in at least two of the three tissue types. A vascular-specific promoter is specifically active in any of the xylem, phloem or cambium, or in at least two of the three. In other words, the promoters are only active in the xylem, cambium or phloem tissue of plants. Note, however, that because of solute transport in plants, a product that is specifically or preferentially expressed in a tissue may be found elsewhere in the plant after expression has occurred.
Additionally, the promoters of particular monolignol synthesis, monolignol transport, and lignin polymerization genes may be expressed only within the cambium in developing secondary vasculature. Within the cambium, particular monolignol synthesis, monolignol transport, and lignin polymerization gene promoters may be expressed exclusively in the stem or in the root. Moreover, the monolignol synthesis, monolignol transport, and lignin polymerization promoters may be expressed only in the spring (for early wood formation) or only in the summer.
A promoter may be operably linked to the polynucleotide. As used in this context, “operably linked” refers to linking a polynucleotide encoding a structural gene to a promoter such that the promoter controls transcription of the structural gene. If the desired polynucleotide comprises a sequence encoding a protein product, the coding region can be operably linked to regulatory elements, such as to a promoter and a terminator, that bring about expression of an associated messenger RNA transcript and/or a protein product encoded by the desired polynucleotide. In this instance, the polynucleotide is operably linked in the 5′- to 3′-orientation to a promoter and, optionally, a terminator sequence. Accordingly, one or more elements can be operably linked in order to control the transcription of a structural gene.
Alternatively, the invention provides DNA constructs comprising a polynucleotide in an “antisense” orientation, the transcription of which produces nucleic acids that can form secondary structures that affect expression of an endogenous monolignol synthesis, monolignol transport or lignin polymerization gene in the plant cell. In another variation, the DNA construct may comprise a polynucleotide that yields a double-stranded RNA product upon transcription that initiates RNA interference of a monolignol synthesis, monolignol transport or lignin polymerization gene with which the polynucleotide is associated. A polynucleotide of the present invention can be positioned within a t-DNA, such that the left and right t-DNA border sequences flank or are on either side of the polynucleotide.
It should be understood that the invention includes DNA constructs comprising one or more of any of the polynucleotides discussed above, e.g., SEQ ID NO: 1-252, 756 and 768. The invention includes DNA constructs comprising one or more of any of the polynucleotides discussed above, e.g., SEQ ID NO: 1-252, 756 and 768, and one or more t-DNA borders that facilitate integration into a plant genome.
The invention also includes DNA constructs comprising a promoter that includes one or more regulatory elements. Alternatively, the invention includes DNA constructs comprising a regulatory element that is separate from a promoter. Regulatory elements confer a number of important characteristics upon a promoter region. Some elements bind transcription factors that enhance the rate of transcription of the operably linked nucleic acid. Other elements bind repressors that inhibit transcription activity. The effect of transcription factors on promoter activity can determine whether the promoter activity is high or low, i.e. whether the promoter is “strong” or “weak.”
A DNA construct of the invention can include a nucleotide sequence that serves as a selectable marker useful in identifying and selecting transformed plant cells or plants. Numerous selectable markers are known in the art. See, e.g., B. Miki and S. McHugh, J. Biotechnol. 107(3):193-232 (2004). Selectable marker genes can confer positive or negative selection of transformed plant cells or plants. Selectable makers genes and gene products can be conditional or non-conditional on the presence of external substrates. As used herein, a “positive selectable marker gene” promotes the growth of transformed tissue. In contrast, a “negative selectable marker gene” results in the death of the transformed tissue. Positive selectable marker genes can be conditional on the use of toxic agents, such as antibiotics, herbicides or drugs. In addition, positive selectable marker genes can be conditional on non-toxic agents that may be substrates for growth or that induce growth and differentiation of the transformed plant cells or plants. Positive selectable marker genes can also alter the physiological processes that govern plant development. Examples of such selectable markers include, but are not limited to, a neomycin phosphotransferase (nptII) gene (Potrykus et al., Mol. Gen. Genet. 199:183-188 (1985)), which confers kanamycin resistance. Cells expressing the nptII gene can be selected using an appropriate antibiotic such as kanamycin or G418. Other commonly used selectable markers include a mutant EPSP synthase gene (Hinchee et al., Bio/Technology 6:915-922 (1988)), which confers glyphosate resistance; and a mutant acetolactate synthase gene (ALS), which confers imidazolinone or sulphonylurea resistance (European Patent Application No. 154,204).
The present invention also includes vectors comprising the DNA constructs discussed above. The vectors can include an origin of replication (replicons) for a particular host cell. Various prokaryotic replicons are known to those skilled in the art, and function to direct autonomous replication and maintenance of a recombinant molecule in a prokaryotic host cell. See, e.g. Sambrook et al., supra.
For example, pMON530 is an Agrobacterium-based plant transformation vector for use in transformation of dicotyledonous plants is plasmid vector (Rogers et al. “Improved vectors for plant transformation: expression cassette vectors and new selectable markers.,” in M
Binary vector pMON505 is a derivative of pMON200 (Rogers et al., supra,) in which the Ti plasmid homology region, LIH, is replaced with a 3.8 kb HindIII to SmaI segment of the mini RK2 plasmid, pTJS75 (Schmidhauser and Helinski. (1985) J. Bacteriol. 164-155). This segment contains the RK2 origin of replication, oriV, and the origin of transfer, oriT, for conjugation into Agrobacterium using the tri-parental mating procedure. Horsch and Klee., Proc. Natl. Acad. Sci. U.S.A., 83:4428 (1986). Plasmid pMON505 retains all the important features of pMON200 including the synthetic multi-linker for insertion of desired DNA fragments, the chimeric NOS/NPTII′/NOS gene for kanamycin resistance in plant cells, the spectinomycin/streptomycin resistance determinant for selection in E. coli and A. tumefaciens, an intact nopaline synthase gene for facile scoring of transformants and inheritance in progeny, and a pBR322 origin of replication for ease in making large amounts of the vector in E. coli. Plasmid pMON505 contains a single T-DNA border derived from the right end of the pTiT37 nopaline-type T-DNA. Southern blot analyses demonstrate that plasmid pMON505 and any DNA that it carries are integrated into the plant genome, that is, the entire plasmid is the T-DNA that is inserted into the plant genome. One end of the integrated DNA is located between the right border sequence and the nopaline synthase gene and the other end is between the border sequence and the pBR322 sequences. A similar mechanism uses the cre recombinase to integrate constructs into the plant genome. See, e.g., Gleave et al., Plant Mol. Biol. 40(2):223-35 (1999).
A particularly useful Ti plasmid cassette vector is pMON17227. This vector is described in WO 92/04449 and contains a gene encoding an enzyme conferring glyphosate resistance (denominated CP4), which is an excellent selection marker gene for many plants, including potato and tomato. The gene is fused to the Arabidopsis EPSPS chloroplast transit peptide (CTP2), and expression is driven by the promoter of choice.
In one embodiment, the present invention utilizes a pWVR8 vector as described in Gleave, Plant Mol. Biol., 20:1203-27 (1992), Wesley et al., Plant J. 27(6):581-90. (2001).
In another embodiment, the inventive materials and techniques are directed to DNA constructs for stacking one or more monolignol synthesis, monolignol transport, and lignin polymerization genes simultaneously in transgenic plant cells and plants. See, e.g., Li et al., Proc. Natl. Acad. Sci. U.S.A. 100:4939-4944 (2003).
C. Transformed Host Cells, Plant Tissue and Plants
The invention also provides host cells which are transformed with the DNA constructs of the invention. As used herein, a host cell refers to the cell in which a polynucleotide of the invention is expressed. Accordingly, a host cell can be an individual cell, a cell culture or cells that are part of an organism. The host cell can also be a portion of an embryo, endosperm, sperm or egg cell, or a fertilized egg. In one embodiment, the host cell is a plant cell.
The present invention further provides transgenic plants comprising the DNA constructs of the invention. The invention includes transgenic plants that are angiosperms or gymnosperms. The DNA constructs of the present invention can be used to transform a variety of plants, both monocotyledonous (e.g. grasses, corn, grains, oat, wheat and barley), dicotyledonous (e.g., Arabidopsis, tobacco, legumes, alfalfa, oaks, eucalyptus, maple), and Gymnosperms (e.g., U.S. Pat. No. 6,518,485), white spruce (Ellis et al., Biotechnology 11:84-89 (1993)), and larch (Huang et al., In Vitro Cell 27:201-207, 1991).
The plants also include turfgrass, wheat, maize, rice, sugar beet, potato, tomato, lettuce, carrot, strawberry, cassaya, sweet potato, geranium, soybean, and various types of woody plants. Woody plants include trees such as palm oak, pine, maple, fir, apple, fig, plum and acacia. Woody plants also include rose and grape vines.
In one embodiment, the DNA constructs of the invention are used to transform woody plants, i.e., trees or shrubs whose stems live for a number of years and increase in diameter each year by the addition of woody tissue. The invention includes methods of transforming plants including eucalyptus and pine species of significance in the commercial forestry industry such as plants selected from the group consisting of Eucalyptus grandis and its hybrids, and Pinus taeda, as well as the transformed plants and wood and wood pulp derived therefrom. Other examples of suitable plants include those selected from the group consisting of Pinus banksiana, Pinus brutia, Pinus caribaea, Pinus clausa, Pinus contorta, Pinus coulteri, Pinus echinata, Pinus eldarica, Pinus ellioti, Pinus jeffreyi, Pinus lambertiana, Pinus massoniana, Pinus monticola, Pinus nigra, Pinus palustris, Pinus pinaster, Pinus ponderosa, Pinus radiata, Pinus resinosa, Pinus rigida, Pinus serotina, Pinus strobus, Pinus sylvestris, Pinus taeda, Pinus virginiana, Abies amabilis, Abies balsamea, Abies concolor, Abies grandis, Abies lasiocarpa, Abies magnifica, Abies procera, Chamaecyparis lawsoniona, Chamaecyparis nootkatensis, Chamaecyparis thyoides, Juniperus virginiana, Larix decidua, Larix laricina, Larix leptolepis, Larix occidentalis, Larix siberica, Libocedrus decurrens, Picea abies, Picea engelmanni, Picea glauca, Picea mariana, Picea pungens, Picea rubens, Picea sitchensis, Pseudotsuga menziesii, Sequoia gigantea, Sequoia sempervirens, Taxodium distichum, Tsuga canadensis, Tsuga heterophylla, Tsuga mertensiana, Thuja occidentalis, Thuja plicata, Eucalyptus alba, Eucalyptus bancroftii, Eucalyptus botryoides, Eucalyptus bridgesiana, Eucalyptus calophylla, Eucalyptus camaldulensis, Eucalyptus citriodora, Eucalyptus cladocalyx, Eucalyptus coccifera, Eucalyptus curtisii, Eucalyptus dalrympleana, Eucalyptus deglupta, Eucalyptus delegatensis, Eucalyptus diversicolor, Eucalyptus dunnii, Eucalyptus ficifolia, Eucalyptus globulus, Eucalyptus gomphocephala, Eucalyptus gunnii, Eucalyptus henryi, Eucalyptus laevopinea, Eucalyptus macarthurii, Eucalyptus macrorhyncha, Eucalyptus maculata, Eucalyptus marginata, Eucalyptus megacarpa, Eucalyptus melliodora, Eucalyptus nicholii, Eucalyptus nitens, Eucalyptus nova-angelica, Eucalyptus obliqua, Eucalyptus occidentalis, Eucalyptus obtusiflora, Eucalyptus oreades, Eucalyptus pauciflora, Eucalyptus polybractea, Eucalyptus regnans, Eucalyptus resinifera, Eucalyptus robusta, Eucalyptus rudis, Eucalyptus saligna, Eucalyptus sideroxylon, Eucalyptus stuartiana, Eucalyptus tereticornis, Eucalyptus torelliana, Eucalyptus urnigera, Eucalyptus urophylla, Eucalyptus viminalis, Eucalyptus viridis, Eucalyptus wandoo, and Eucalyptus youmanni.
As used herein, the term “plant” also is intended to include the fruit, seeds, flower, strobilus, etc. of the plant. A transformed plant of the current invention can be a direct transfectant, meaning that the DNA construct was introduced directly into the plant, such as through particle bombardment or by Agrobacterium-mediated transformation, or the plant can be the progeny of a transfected plant. The second or subsequent generation plant can be produced by sexual reproduction, i.e., fertilization. Furthermore, the plant can be a gametophyte (haploid stage) or a sporophyte (diploid stage).
As used herein, the term “plant tissue” encompasses any portion of a plant, including plant cells. Plant cells include suspension cultures, callus, embryos, meristematic regions, callus tissue, leaves, roots, shoots, gametophytes, sporophytes, pollen, seeds and microspores. Plant tissues can be grown in liquid or solid culture, or in soil or suitable media in pots, greenhouses or fields. As used herein, “plant tissue” also refers to a clone of a plant, seed, progeny, or propagule, whether generated sexually or asexually, and descendents of any of these, such as cuttings or seeds.
In one aspect of the invention, somatic embryogenesis can be used for the clonal propagation of the inventive transgenic plants and plant tissue. See, e.g., S. A. Merkle and J. F. Dean, Curr. Opin. Biotechnol. 11(3):298-302 (2000).
Likewise, the regeneration of plants is well established for many species. See Dunsten et al., Somatic embryogenesis in woody plants, In in vitro embryogenesis of plants (Current Plant Science and Biotechnology in Agriculture, 12), Kluwer Academic Publishers, Boston, Mass. (1995).
As used herein, “transformation” refers to a process by which a nucleic acid is inserted or incorporated into the genome of a plant cell. Such insertion encompasses stable introduction into the plant cell and transmission to progeny. Transformation also refers to transient insertion of a nucleic acid, wherein the resulting transformant transiently expresses the nucleic acid. Transformation can occur under natural or artificial conditions using various methods well known in the art. See, e.g., Glick and Thompson, eds., M
Plant transformation strategies are described in, for example, U.S. Pat. Nos. 5,159,135 (cotton), 5,981,840 (corn), 5,914,451 (soybean), and WO 00/12715 (eucalyptus), which are incorporated by reference in their entirety. Additional plant transformation strategies and techniques are reviewed in Birch, R. G., Ann. Rev. Plant Physiol. Plant Mol. Biol. 48:297 (1997) and Forester et al., Exp. Agric. 33:15-33 (1997), and are incorporated by reference in their entirety.
Methods for transforming tree species are known in the art. In accordance with one embodiment of the invention, genotype-independent transformation of Eucalyptus explants and generation of transgenic progeny can be accomplished by transformation using Agrobacterium. A tree explant can be, although need not be, harvested and cultured on a pre-culture medium before transformation. Although a pre-culture medium is not necessary, use of such a medium can increase transformation efficiency and plant regeneration. A pre-culture medium is a nutrient medium upon which plant explants can be cultured before transformation with Agrobacterium. Any pre-culture media and time periods of culture can be used. The pre-culture medium contains an Agrobacterium inducer, such as acetosyringone. The pre-culture medium can optionally contain plant growth regulators, including auxin and cytokinin. Pre-culture medium can be prepared using and appropriate salt medium, including, but not limited to Woody Plant Medium (WPM) salts (Lloyd and McCown, Combined Proceedings of the International Plant Propagators Society, 30:421-427, 1980), Murashige and Skoog medium (Sigma Aldrich, St. Louis, Mo.) or Lepoivre medium. The pre-culture medium can contain Agrobacterium inducers, such as, for example acetosyringone. Optionally, pre-culture medium can contain auxin, cytokinin, or both auxin and cytokinin. An exemplary plant pre-culture medium is shown below.
Amount per Liter
Medium Components
of Medium
WPM salts
1 package
(Sigma)
Ca(NO3)2•4H2O
3.7
g
MgSO4•4H2O
0.37
g
Nicotinic Acid
0.5
mg
Thiamine•HCl
0.5
mg
Pyridoxin•HCl
0.5
mg
D-Pantothenic Acid
1.0
mg
Myo-inositol
0.1
g
BA
0.1-1
mg
Bacto-agar
5-8
g
Acetosyringone
5-200
mg
NAA
0.2-3
mg
zeatin
1-6
mg
In this transformation method, plant explants can be pre-cultured for four days in the dark on the pre-culture medium. Induced Agrobacterium culture can be prepared by methods known in the art. The induced culture is applied to a plant explant. Explants can be transformed by application of Agrobacterium culture to the explant, vacuum infiltration, floral dip, etc. Following transformation, Agrobacterium culture-treated explants can be co-cultivated with Agrobacterium under light or dark conditions for 2-10 days. In one embodiment, the explants are co-cultivated with Agrobacterium under light or dark conditions for 4 days.
Following co-cultivation, explants can be transferred to regeneration medium with 400 mg/L timentin. Explants can be cultured on regeneration medium before transfer to a selection medium. In one embodiment, explants are cultured on regeneration medium for four days. Any suitable selection medium can be used. In one embodiment, the selection medium is the regeneration medium supplemented with both timentin and an herbicide selection agent. The table below provides an exemplary regeneration medium.
Components for 1 Liter of Medium
Grams
KNO3
1
NH4H2PO4
0.25
MgSO4•7H2O
0.25
CaCl2•2H2O
0.10
FeSO4•7H2O
0.0139
Na2EDTA•2H2O
0.01865
MES (Duchefa m1501)
600.0
MS Micro (1/2 strength)
MnSO4•H2O
0.00845
ZnSO4•7H2O
0.0043
CuSO4•5H2O
0.0000125
CoCl2•6H2O
0.0000125
KI
0.000415
H3BO3
0.0031
Na2MoO4•2H2O
0.000125
Plant Growth Regulators
Zeatin
NAA (naphthalene acetic acid)
Sugars
Glucose/Sucrose
20.0
Myo-inositol
0.100
Amino Acid and Vitamin Mix
Nicotinic Acid
0.010
Thiamine
0.010
Ca Pantothenate
0.001
Pyridoxine
0.001
Biotin
0.00001
Ascorbic Acid
0.050
L-glutamine
0.1
Arginine
0.0258
Glycine
0.00199
Lysine
0.0508
Methionine
0.0132
Phenylalanine
0.0257
Serine
0.00904
Threonine
0.00852
Tryptophan
0.0122
Tyrosine
0.0127
Gelling Agent
Gelrite
3.0
Shoot clumps that survive selection are maintained on regeneration medium containing herbicide and timentin. The shoot clumps can be transferred until shoots proliferate and initially elongate. In one embodiment, the shoot clumps are transferred every 3 weeks.
Any reporter gene can be used, such as, for example, GFP, luciferase, or GUS. See, e.g., B. Miki and S. McHugh, J. Biotechnol. 107(3):193-232 (2004).
In one embodiment, GUS staining can performed to monitor the frequency of Agrobacterium infection and to ensure that the selected shoots are not escapes or chimeras. Leaf and stem tissues from the regenerated shoots can be stained for reporter gene expression immediately upon shoot development. For example, to determine GUS activity, the explants can be incubated in a substrate comprising 100 mM phosphate buffer (pH 7.0), 0.05% dimethyl suphoxide, 0.05% Triton X-100, 10 mM EDTA, 0.5 mM potassium ferrocyanide, and 1.5 mg/ml 5-bromo-4-chloro-3-indolyl-β-D-glucuronide (X-gluc). The explants can then be subjected to 10 minutes of vacuum before an overnight incubation at 37° C. prior to counting GUS foci.
In accordance with another embodiment, transformation of Pinus is accomplished using the methods described in U.S. Patent Application Publication No. 2002/0100083.
D. Modulation of Plant Phenotype
In accordance with another aspect of the invention, a transgenic plant that has been transformed with a DNA construct of the invention has a phenotype that is different from a plant that has not been transformed with the DNA construct.
As used herein, “phenotype” refers to a distinguishing feature or characteristic of a plant which can be altered according to the present invention by integrating one or more DNA constructs of the invention into the genome of at least one plant cell of a plant. The DNA construct can confer a change in the phenotype of a transformed plant by modifying any one or more of a number of genetic, molecular, biochemical, physiological, morphological, or agronomic characteristics or properties of the transformed plant cell or plant as a whole.
1. Modulating Lignin Content, Lignin Compositions and Various Economic and Non-Economic Traits
In one embodiment, transformation of a plant with an inventive DNA contruct can yield a phenotype including, but not limited to, increased or decreased lignin content or lignin composition. As used herein, “lignin content” referes to the relative amount of lignin polymer present relative to nonlignin components of the plant such as, for example, cellulose, hemicellulose, or nonlignin cell wall phenolics.
In contrast and as used herein, “lignin composition” refers to the relative percentages of each lignin subunit, i.e., p-hydroxyphenyl, guaiacyl, and syringyl, among others. The inventive methods are used to modulate the relative percentages of each subunit monomer in the final polymerized lignin, i.e., change the syringyl-to-guaiacyl ratio (S/G ratio). In one embodiment, the inventive methods are used to direct the production and incorporation of sinapyl alcohol so that the lignin of a transformed plant comprises a greater percentage of syringyl monomers than a wild-type plant. In a further embodiment, the inventive methods comprise directing the production of sinapyl alcohol in a transformed plant which would otherwise have lignin with little to no syringyl monomers.
In one embodiment, transformation of a plant with a DNA construct of the present invention can yield a phenotype including, but not limited to any one or more of increased drought tolerance, herbicide resistance, reduced or increased height, reduced or increased branching, enhanced cold and frost tolerance, improved vigor, enhanced or altered color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced resistance of the wood to decay, enhanced resistance to fungal diseases, altered attractiveness to insect pests, increased disease tolerance, increased insect tolerance, increased water-stress tolerance, improved texture, increased germination, increased micronutrient uptake, production of novel resins, and production of novel proteins or peptides.
In another embodiment, the affected phenotype includes one or more of the following traits: propensity to form reaction wood (i.e., compression wood and tension wood), a reduced period of juvenility, an increased period of juvenility, self-abscising branches, accelerated or delayed reproductive development, as compared to a plant of the same species that has not been transformed with the DNA construct.
In a further embodiment, the phenotype that is different in the transgenic plant includes one or more of the following: lignin quality, lignin structure, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization and accumulation, fiber dimensions, lumen size, proportion of rays, proportion of vessel elements, proportion of nonlignin cell wall phenolics, other plant components, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape.
2. Assessment of Phenotypic Change
Phenotype can be assessed by any suitable means. The plants can be evaluated based on their general morphology. Transgenic plants can be observed with the naked eye, can be weighed and their height measured. The plant can be examined by isolating individual layers of plant tissue, namely phloem and cambium, which is further sectioned into meristematic cells, early expansion, late expansion, secondary wall formation, and late cell maturation. See, e.g., Hertzberg, supra. The plants also can be assessed using microscopic analysis or chemical analysis.
Microscopic analysis includes examining cell types, stage of development, and stain uptake by tissues and cells. Fiber morphology, such as fiber wall thickness and microfibril angle of wood pulp fibers can be observed using, for example, microscopic transmission ellipsometry. See Ye and Sundström, Tappi J., 80:181 (1997). Wood strength, density, and grain slope in wet wood and standing trees can be determined by measuring the visible and near infrared spectral data in conjunction with multivariate analysis. See, U.S. Patent Application Publication Nos. 2002/0107644 and 2002/0113212. Lumen size can be measured using scanning electron microscopy. Lignin structure and chemical properties can be observed using nuclear magnetic resonance spectroscopy as described in Marita et al., J. Chem. Soc., Perkin Trans. I 2939 (2001).
The biochemical characteristic of lignin, cellulose, carbohydrates and other plant extracts can be evaluated by any standard analytical method known including spectrophotometry, fluorescence spectroscopy, HPLC, mass spectroscopy, and tissue staining methods. See, e.g., R. J. Evans and T. A. Milne, Energy & Fuels 1(2):123-137 (1987).
The technique of molecular-beam, mass spectrometric (MBMS) sampling is particularly useful for the characterization of the cellulose, lignin and hemicellulose components of wood. See Evans and Milne, supra.
Techniques for the quantification of lignin content are well known to the skilled artisan. Acetyl bromide extraction (ABE) can be used to quantify lignin. ABE involves the extraction of lignin using aceyl bromide followed by the spectrophotometric measuring the absorbance of the extracted lignin at 280 nm. See K. Liyama and A. F. A. Wallis, Wood Sci. Technol. 22:271-280 (1988). Klason lignin determination is a method to quantify lignin consisting of hydrolyzing the cell wall polysaccharides with sulfuric acid. This leaves the lignin as an insoluble material which is dried and quantified gravimetriclly. See M. J. Effland, T.A.P.P.I. 60:143-144 (1977). Thioglycolic acid extraction (TAE) can be used to quantify lignin. In this method, lignin is extracted using tioglycolic acid and alkali and then measured spectrophotometrically. See Campbell, M. M. and B. E. Ellis, Plant Physiol. 98:62-70 (1992).
A skilled artisan also can use several methods to determine the lignin composition of the inventive transgenic plant cells and plants. Alkaline nitrobenzene oxidation (ANO) or culpric oxide oxidation can be used to determine lignin composition. See, e.g., Dence et al. (1992) Methods of Lignin Chemistry, Springer-Verlag, New York, N.Y. In ANO, lignin is oxidized with nitro benzene in alkali and the degredation products are measured after HPLC separation or gas chromatography. A skilled artisan can used derivation followed by reductive cleavage (DFRC) to determine lignin composition. In DFRC, the alpha- and beta-aryl ether linkages in lignin are cleaved by acetyle bromide and the released cinnamyl acetates are quantified by gas chromatography. See Lu, F. and J. Ralph, J. Agric. Food Chem. 45:2590-2592 (1997). Lignin composition can also be determined using fourier transform infrared (FTIR) and diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy. Both FTIR and DRIFT rely an the absorption of energy from an illuminating laser. In FTIR, a ratio of absorbance intensities at different wavelengths is related to the concentration of different molecules in a sample. In DRIFT, absorbance spectra is generated by light reflecting from the surface of opaque materials. NMR spectroscopy can also provide information as to the composition of isolated lignin fractions. NMR allows the characterization of each lignin subunit (i.e., p-hydroxyphenyl, guaiacyl, and syringyl), the determination of functional groups (i.e., methoxy and hydroxyl), and the characterization of the main inter-subunit bonds. Thioacidolysis in yet another method for determining lignin composition. Thioacidolysis and subsequent gas chromatography can identify monomers that are released by selective breaking of the main inter-subunit bonds. This method is specific for phenylpropanoids and is very sensitive. See Lapierre et al., Plant Physiol. 119:153-163 (1999); Boudet et al., New Phytol. 129:203-236 (1995).
E. Compositions and Methods for Enhancing Wood or Wood Pulp
Another aspect of the invention provides methods of obtaining wood and/or making wood pulp from a plant transformed with a DNA construct of the invention. Methods of producing a transgenic plant are provided above and are known in the art. A transformed plant can be cultured or grown under any suitable conditions. For example, pine can be cultured and grown as described in U.S. Patent Application Publication No. 2002/0100083. Eucalyptus can be cultured and grown as in, for example, Rydelius, et al., “Growing Eucalyptus for Pulp and Energy,” presented at the Mechanization in Short Rotation, Intensive Culture Forestry Conference, Mobile, Ala., 1994. Wood and wood pulp can be obtained from the plant by any means known in the art. For example, pulping processes known in the art include, but are not limited to mechanical pulping, thermomechanical pulping, enzymatic pulping, chemical pulping, or chemithermomechanical pulping. Moreover, multiple techniques of each pulping process are known, e.g., known chemical pulping process include acidic or bisulfate pulping, sulfate pulping, Kraft pulping, soda pulping, anthraquinone pulping, or Kraft-anthraquinone pulping.
As noted above, the wood or wood pulp obtained in accordance with this invention can demonstrate improved characteristics including, but not limited to any one or more of lignin composition, lignin structure, wood composition, cellulose polymerization, fiber dimensions, ratio of fibers to other plant components, increased or decreased nonlignin cell wall phenolics, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, rate of wood formation, aesthetic appearance of wood, formation of stem defects, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape.
In other embodiments, the inventive wood or wood pulp can demonstrate improved characteristics, including increased or decreased lignin content, increased accessibility of lignin to chemical treatments, improved reactivity of lignin, increased or decreased cellulose content increased dimensional stability, increased tensile strength, increased shear strength, increased compression strength, increased shock resistance, increased stiffness, increased or decreased hardness, decreased spirality, decreased shrinkage, and differences in weight, density, and specific gravity.
In yet another embodiment, the inventive wood or wood pulp comprises lignin of an altered S/G ratio, an increased S/G ratio, or a decreased S/G ratio, as compared to wood or wood pulp from a wild-type plant. Specifically, the inventive wood or wood pulp can comprise lignin with increased S/G ratio such that the wood or wood pulp degrades faster than that from a wild-type plant. In another embodiment, the inventive wood or wood pulp can comprise lignin with increased S/G ratio such that the wood or wood pulp more efficiently undergoes delignification. In one embodiment, the inventive methods are used to direct the production and incorporation of sinapyl alcohol so that the lignin of a transformed plant comprises a greater percentage of syringyl monomers than a corresponding non-transformed plant. In another embodiment, the inventive methods are used to increase the lignin content of a transformed plant about at least 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 55%, 60%, 65%, and 70%, as compared to a corresponding non-transformed plant. In another embodiment, the inventive methods are used to decrease the lignin content of a transformed plant about at least 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 55%, 60%, 65%, and 70%, as compared to a corresponding non-transformed plant. In yet another embodiment, the inventive methods are used to alter the lignin composition by increasing the relative percentage of syringyl lignin of a transformed plant about at least 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 55%, 60%, 65%, and 70%, as compared to a corresponding non-transformed plant. In another embodiment, the inventive methods are used to alter the lignin composition by decreasing the relative percentage of syringyl lignin of a transformed plant about at least 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%, 50%, 55%, 60%, 65%, and 70%, as compared to a corresponding non-transformed plant. Those skilled in the art would understand that lignin levels vary in different species, clones and plantings.
Delignification can occur by one or more processes known in the art. The lignin can be removed using the Kraft pulping process. The Kraft process uses both sodium hyrdroxide and sodium sulfide as delignifying agents. As the wood pulp is heated, the sodium sulfide is hydrolyzed and the different sulfur compounds react with lignin to form more soluable thiolignins. Delignification can occur by the use of soda pupling (i.e., the use of sodium hydroxide in the pulping liquor). Likewise, delignification processes can make use of quinonic compounds, such as anthraquinone.
In one embodiment, the methods of the invention can be used to decrease the lignin content of wood pulp. As used herein, a “kappa number” refers to a measure of the residual lignin in wood pulp. The kappa number can be obtained by measuring the comsumption of permanganate ions that react with lignin in the pulp. Accordingly, lower kappa numbers are associated with lower levels of lignin content in wood pulp. In other embodiment, the methods of the invention can be used to increase the lignin content of wood pulp.
In other embodiments, the methods of the invention can be used to decrease the Klason lignin content of wood and wood pulp. See M. J. Effland, T.A.P.P.I. 60:143-144 (1977). In another embodiment, the methods of the invention can be used to increase the Klason lignin content of wood and wood pulp.
III. Expression Profiling of Monolignol Synthesis, Monolignol Transportation, and Lignin Polymerization
The present invention also provides methods and tools for performing expression profiling of monolignol synthesis, monolignol transportation, and lignin polymerization genes. Expression profiling is useful in determining whether genes are transcribed or translated, comparing transcript levels for particular genes in different tissues, genotyping, estimating DNA copy number, determining identity of descent, measuring mRNA decay rates, identifying protein binding sites, determining subcellular localization of gene products, correlating gene expression to a phenotype or other phenomenon, and determining the effect on other genes of the manipulation of a particular gene. Expression profiling is particularly useful for identifying gene expression in complex, multigenic events, such as the lignification process. For this reason, expression profiling is useful in correlating monolignol synthesis, monolignol transportation, and lignin polymerization gene expression to plant phenotype and formation of plant tissues and the interconnection thereof to the lignification process.
Only a small fraction of a plant's monolignol synthesis, monolignol transportation, and lignin polymerization genes are expressed at a given time in a given tissue sample, and all of the expressed genes may not affect the plant phenotype. To identify genes capable of affecting a phenotype of interest, the present invention provides methods and tools for determining, for example, a monolignol synthesis, monolignol transportation, and lignin polymerization gene expression profile at a given point in plant development and a monolignol synthesis, monolignol transportation, and lignin polymerization gene expression profile a given tissue sample. The invention also provides methods and tools for identifying monolignol synthesis, monolignol transportation, and lignin polymerization genes whose expression can be manipulated to alter plant phenotype. In support of these methods, the invention also provides methods and tools that distinguish expression of different genes of the same family, such as methyltransferases and peroxidases.
As used herein, “gene expression” refers to the process of transcription of a DNA sequence into an RNA sequence, followed by translation of the RNA into a protein, which may or may not undergo post-translational processing. Thus, the relationship between plant phenotype and monolignol synthesis, monolignol transportation, and lignin polymerization gene expression can be observed by detecting, quantitatively or qualitatively, changes in the level of an RNA or a protein. As used herein, the term “biological activity” includes, but is not limited to, the activity of a protein gene product, including enzyme activity, such as, for example, methyltransferase activity.
The present invention provides oligonucleotides that are useful in these expression profiling methods. Each oligonucleotide is capable of hybridizing under a given set of conditions to a monolignol synthesis, monolignol transport, or lignin polymerization gene or gene product. In one aspect of the invention, a plurality of oligonucleotides is provided, wherein each oligonucleotide hybridizes under a given set of conditions to a different monolignol synthesis, monolignol transport, or lignin polymerization gene product. Examples of oligonucleotides of the present invention include SEQ ID NOs: 505-756, 767 and 770. Each of the oligonucleotides of SEQ ID NOs 505-756, 767 and 770 hybridizes under standard conditions to a different gene product of one of SEQ ID NOs: 1-252, 765 and 768. The oligonucleotides of the invention are useful in determining the expression of one or more monolignol synthesis, monolignol transport, or lignin polymerization genes in any of the above-described methods.
A. Cell, Tissue, Nucleic Acid and Protein Samples
Samples for use in methods of the present invention may be derived from plant tissue. Suitable plant tissues include, but are not limited to, somatic embryos, pollen, leaves, stems, calli, stolons, microtubers, shoots, xylem, male strolbili, female strolbili, pollen cones, vascular tissue, apical meristem, vascular cambium, xylem, root, flower, and seed.
According to the present invention “plant tissue” is used as described previously herein. Plant tissue can be obtained from any of the plants types or species described supra.
In accordance with one aspect of the invention, samples can be obtained from plant tissue at different developmental stages, from plant tissue at various times of the year (e.g. spring versus summer), from plant tissues subject to different environmental conditions (e.g. variations in light and temperature) and/or from different types of plant tissue and cells. In accordance with one embodiment, plant tissue is obtained during various stages of maturity and during different seasons of the year. In a further embodiment, plant tissue is obtained from plants displaying different phenotypes. For example, plant tissue can be collected from stem dividing cells, differentiating xylem, early developing wood cells, differentiated early wood cells, and differentiated late wood cells. As another example, gene expression in a sample obtained from a plant with developing wood can be compared to gene expression in a sample obtained from a plant which does not have developing wood. As a further example, gene expression in a sample obtained from a plant displaying a reaction wood phenotype, such as compression wood or tension wood, can be compared to gene expression in a sample obtained from a plant which does not have reaction wood.
Differentiating xylem includes samples obtained from reaction wood. Reaction wood includes compression wood, side-wood, tension wood, and normal vertical xylem. Methods of obtaining samples for expression profiling from pine and eucalyptus are known. See, e.g., Allona et al., Proc. Nat'l Acad. Sci. 95:9693-8 (1998) and Whetton et al., Plant Mol. Biol. 47:275-91, and Kirst et al., Int'l Union of Forestry Research Organizations Biennial Conference, S6.8 (June 2003, Umea, Sweden).
In one embodiment of the invention, gene expression in one type of tissue is compared to gene expression in a different type of tissue or to gene expression in the same type of tissue in a difference stage of development. Gene expression can also be compared in one type of tissue which is sampled at various times during the year (different seasons). For example, gene expression in juvenile secondary xylem can be compared to gene expression in mature secondary xylem. Similarly, gene expression in cambium can be compared to gene expression in xylem. Furthermore, gene expression in apical meristems can be compared to gene expression in cambium.
In another embodiment of the invention, a sample is obtained from a plant having a specific phenotype and gene expression in that sample is compared to a sample obtained from a plant of the same species that does not have that phenotype. For example, a sample can be obtained from a plant exhibiting a fast rate of growth and gene expression can be compared with that of a sample obtained from a plant exhibiting a normal or slow rate of growth. Differentially expressed genes identified from such a comparison can be correlated with growth rate and, therefore, useful for manipulating growth rate.
In a further embodiment, a sample is obtained from clonally propagated plants. In one embodiment the clonally propagated plants are of the species Pinus or Eucalyptus. Individual ramets from the same genotype can be sacrificed at different times of year. Thus, for any genotype there can be at least two genetically identical trees sacrificed, early in the season and late in the season. Each of these trees can be divided into juvenile (top) to mature (bottom) samples. Further, tissue samples can be divided into, for example, phloem to xylem, in at least 5 layers of peeling. Each of these samples can be evaluated for phenotype and gene expression.
Where cellular components may interfere with an analytical technique, such as a hybridization assay, enzyme assay, a ligand binding assay, or a biological activity assay, it may be desirable to isolate the gene products from such cellular components. Gene products, including nucleic acid and amino acid gene products, can be isolated from cell fragments or lysates by any method known in the art.
Nucleic acids used in accordance with the invention can be prepared by any available method or process, or by other processes as they become known in the art. Conventional techniques for isolating nucleic acids are detailed, for example, in Tijssen, L
A suitable nucleic acid sample can contain any type of nucleic acid derived from the transcript of a monolignol synthesis, monolignol transport, or lignin polymerization gene, i.e., RNA or a subsequence thereof or a nucleic acid for which an mRNA transcribed from a monolignol synthesis, monolignol transport, or lignin polymerization gene served as a template. Suitable nucleic acids include cDNA reverse-transcribed from a transcript, RNA transcribed from that cDNA, DNA amplified from the cDNA, and RNA transcribed from the amplified DNA. Detection of such products or derived products is indicative of the presence and/or abundance of the transcript in the sample. Thus, suitable samples include, but are not limited to, transcripts of the gene or genes, cDNA reverse-transcribed from the transcript, cRNA transcribed from the cDNA, DNA amplified from the genes, and RNA transcribed from amplified DNA. As used herein, the category of “transcripts” includes but is not limited to pre-mRNA nascent transcripts, transcript processing intermediates, and mature mRNAs and degradation products thereof.
It is not necessary to monitor all types of transcripts to practice the invention. For example, the expression profiling methods of the invention can be conducted by detecting only one type of transcript, such as mature mRNA levels only.
In one aspect of the invention, a chromosomal DNA or cDNA library (comprising, for example, fluorescently labeled cDNA synthesized from total cell mRNA) is prepared for use in hybridization methods according to recognized methods in the art. See Sambrook et al., supra.
In another aspect of the invention, mRNA is amplified using, e.g., the MessageAmp kit (Ambion). In a further aspect, the mRNA is labeled with a detectable label. For example, mRNA can be labeled with a fluorescent chromophore, such as CyDye (Amersham Biosciences).
In some applications, it may be desirable to inhibit or destroy RNase that often is present in homogenates or lysates, before use in hybridization techniques. Methods of inhibiting or destroying nucleases are well known. In one embodiment of the invention, cells or tissues are homogenized in the presence of chaotropic agents to inhibit nuclease. In another embodiment, RNase is inhibited or destroyed by heat treatment, followed by proteinase treatment.
Protein samples can be obtained by any means known in the art. Protein samples useful in the methods of the invention include crude cell lysates and crude tissue homogenates. Alternatively, protein samples can be purified. Various methods of protein purification well known in the art can be found in Marshak et al., S
B. Detecting Levels of Gene Expression
For methods of the invention that comprise detecting a level of gene expression, any method for observing gene expression can be used, without limitation. Such methods include traditional nucleic acid hybridization techniques, polymerase chain reaction (PCR) based methods, and protein determination. The invention includes detection methods that use solid support-based assay formats as well as those that use solution-based assay formats.
Absolute measurements of the expression levels need not be made, although they can be made. The invention includes methods comprising comparisons of differences in expression levels between samples. Comparison of expression levels can be done visually or manually, or can be automated and done by a machine, using for example optical detection means. Subrahmanyam et al., Blood. 97: 2457 (2001); Prashar et al., Methods Enzymol. 303: 258 (1999). Hardware and software for analyzing differential expression of genes are available, and can be used in practicing the present invention. See, e.g., GenStat Software and GeneExpress® GX Explorer™ Training Manual, supra; Baxevanis & Francis-Ouellette, supra.
In accordance with one embodiment of the invention, nucleic acid hybridization techniques are used to observe gene expression. Exemplary hybridization techniques include Northern blotting, Southern blotting, solution hybridization, and S1 nuclease protection assays.
Nucleic acid hybridization typically involves contacting an oligonucleotide probe and a sample comprising nucleic acids under conditions where the probe can form stable hybrid duplexes with its complementary nucleic acid through complementary base pairing. For example, see PCT application WO 99/32660; Berger & Kimmel, Methods Enzymol. 152: 1 (1987). The nucleic acids that do not form hybrid duplexes are then washed away leaving the hybridized nucleic acids to be detected, typically through detection of an attached detectable label. The detectable label can be present on the probe, or on the nucleic acid sample. In one embodiment, the nucleic acids of the sample are detectably labeled polynucleotides representing the mRNA transcripts present in a plant tissue (e.g., a cDNA library). Detectable labels are commonly radioactive or fluorescent labels, but any label capable of detection can be used. Labels can be incorporated by several approached described, for instance, in WO 99/32660, supra. In one aspect RNA can be amplified using the MessageAmp kit (Ambion) with the addition of aminoallyl-UTP as well as free UTP. The aminoallyl groups incorporated into the amplified RNA can be reacted with a fluorescent chromophore, such as CyDye (Amersham Biosciences)
Duplexes of nucleic acids are destabilized by increasing the temperature or decreasing the salt concentration of the buffer containing the nucleic acids. Under low stringency conditions (e.g., low temperature and/or high salt) hybrid duplexes (e.g., DNA:DNA, RNA:RNA or RNA:DNA) will form even where the annealed sequences are not perfectly complementary. Thus, specificity of hybridization is reduced at lower stringency. Conversely, at higher stringency (e.g., higher temperature and/or lower salt and/or in the presence of destabilizing reagents) hybridization tolerates fewer mismatches.
Typically, stringent conditions for short probes (e.g., 10 to 50 nucleotide bases) will be those in which the salt concentration is at least about 0.01 to 1.0 M at pH 7.0 to 8.3 and the temperature is at least about 30° C. Stringent conditions can also be achieved with the addition of destabilizing agents such as formamide.
Under some circumstances, it can be desirable to perform hybridization at conditions of low stringency, e.g., 6×SSPE-T (0.9 M NaCl, 60 mM NaH2PO4, pH 7.6, 6 mM EDTA, 0.005% Triton) at 37° C., to ensure hybridization. Subsequent washes can then be performed at higher stringency (e.g., 1×SSPE-T at 37° C.) to eliminate mismatched hybrid duplexes. Successive washes can be performed at increasingly higher stringency (e.g., down to as low as 0.25×SSPE-T at 37° C. to 50° C.) until a desired level of hybridization specificity is obtained.
In general, standard conditions for hybridization is a compromise between stringency (hybridization specificity) and signal intensity. Thus, in one embodiment of the invention, the hybridized nucleic acids are washed at successively higher stringency conditions and read between each wash. Analysis of the data sets produced in this manner will reveal a wash stringency above which the hybridization pattern is not appreciably altered and which provides adequate signal for the particular oligonucleotide probes of interest. For example, the final wash may be selected as that of the highest stringency that produces consistent results and that provides a signal intensity greater than approximately 10% of the background intensity.
1. Oligonucleotide Probes
Oligonucleotide probes useful in nucleic acid hybridization techniques employed in the present invention are capable of binding to a nucleic acid of complementary sequence through one or more types of chemical bonds, usually through complementary base pairing via hydrogen bond formation. A probe can include natural bases (i.e., A, G, U, C or T) or modified bases (7-deazaguanosine, inosine, etc.). In addition, the nucleotide bases in the probes can be joined by a linkage other than a phosphodiester bond, so long as it does not interfere with hybridization. Thus, probes can be peptide nucleic acids in which the constituent bases are joined by peptide bonds rather than phosphodiester linkages.
Oligonucleotide probes can be prepared by any means known in the art. Probes useful in the present invention are capable of hybridizing to a nucleotide product of a monolignol synthesis, monolignol transport, or lignin polymerization gene, such as one of SEQ ID NOs: 1-252, 765 and 768. Probes useful in the invention can be generated using the nucleotide sequences disclosed in SEQ ID NOs: 1-252, 765 and 768. The invention includes oligonucleotide probes having at least a 2, 10, 15, 20, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, or 100 nucleotide fragment of a corresponding contiguous sequence of any one of SEQ ID NOs: 1-252, 765 and 768. The invention includes oligonucleotides of less than 2, 1, 0.5, 0.1, or 0.05 kb in length. In one embodiment, the oligonucleotide is 60 nucleotides in length. In another embodiment, the oligonucleotide is 30 nucleotides in length.
Oligonucleotide probes can be designed by any means known in the art. See, e.g., Li and Stormo, Bioinformatics 17: 1067-76 (2001). Oligonucleotide probe design can be effected using software. Exemplary software includes ArrayDesigner, GeneScan, and ProbeSelect. Probes complementary to a defined nucleic acid sequence can be synthesized chemically, generated from longer nucleotides using restriction enzymes, or can be obtained using techniques such as polymerase chain reaction (PCR). PCR methods are well known and are described, for example, in Innis et al. eds., PCR P
The invention includes oligonucleotide probes that hybridize to a product of the coding region or a 3′ untranslated region (3′ UTR) of a monolignol synthesis, monolignol transport, or lignin polymerization gene. In one embodiment, the oligonucleotide probe hybridizes to the 3′UTR of any one of SEQ ID NOs: 1-29. The 3′ UTR is generally a unique region of the gene, even among members of the same family. Therefore, the probes capable of hybridizing to a product of the 3′ UTR can be useful for differentiating the expression of individual genes within a family where the coding region of the genes likely are highly homologous. This allows for the design of oligonucleotide probes to be used as members of a plurality of oligonucleotides, each capable of uniquely binding to a single gene. In another embodiment, the oligonucleotide probe comprises any one of SEQ ID NOs: 505-756, 767 and 770. In another embodiment, the oligonucleotide probe consists of any one of SEQ ID NOs: 1-252, 765 and 768.
2. Oligonucleotide Array Methods
One embodiment of the invention employs two or more oligonucleotide probes in combination to detect a level of expression of one or more monolignol synthesis, monolignol transport, and lignin polymerization genes, such as the genes of SEQ ID NOs: 1-252, 765 and 768. In one aspect of this embodiment, the level of expression of two or more different genes is detected. The two or more genes may be from the same or different monolignol synthesis, monolignol transport, and lignin polymerization gene families discussed above. Each of the two or more oligonucleotides may hybridize to a different one of the genes.
One embodiment of the invention employs two or more oligonucleotide probes, each of which specifically hybridize to a polynucleotide derived from the transcript of a gene provided by SEQ ID NOs: 1-252, 765 and 768. Another embodiment employs two or more oligonucleotide probes, at least one of which comprises a nucleic acid sequence of SEQ ID NOs: 505-756, 767 and 770. Another embodiment employs two or more oligonucleotide probes, at least one of which consists of SEQ ID NOs: 505-756, 767 and 770.
The oligonucleotide probes may comprise from about 5 to about 60, or from about 5 to about 500, nucleotide bases, such as from about 60 to about 100 nucleotide bases, including from about 15 to about 60 nucleotide bases.
One embodiment of the invention uses solid support-based oligonucleotide hybridization methods to detect gene expression. Solid support-based methods suitable for practicing the present invention are widely known and are described, for example, in PCT application WO 95/11755; Huber et al., Anal. Biochem. 299: 24 (2001); Meiyanto et al., Biotechniques. 31: 406 (2001); Relogio et al., Nucleic Acids Res. 30:e51 (2002). Any solid surface to which oligonucleotides can be bound, covalently or non-covalently, can be used. Such solid supports include filters, polyvinyl chloride dishes, silicon or glass based chips, etc.
One embodiment uses oligonucleotide arrays, i.e. microarrays, which can be used to simultaneously observe the expression of a number of genes or gene products. Oligonucleotide arrays comprise two or more oligonucleotide probes provided on a solid support, wherein each probe occupies a unique location on the support. The location of each probe may be predetermined, such that detection of a detectable signal at a given location is indicative of hybridization to an oligonucleotide probe of a known identity. Each predetermined location can contain more than one molecule of a probe, but each molecule within the predetermined location has an identical sequence. Such predetermined locations are termed features. There can be, for example, from 2, 10, 100, 1,000, 2,000 or 5,000 or more of such features on a single solid support. In one embodiment, each oligonucleotide is located at a unique position on an array at least 2, at least 3, at least 4, at least 5, at least 6, or at least 10 times.
Oligonucleotide probe arrays for detecting gene expression can be made and used according to conventional techniques described, for example, in Lockhart et al., Nat'l Biotech. 14: 1675 (1996), McGall et al., Proc. Nat'l Acad. Sci. USA 93: 13555 (1996), and Hughes et al., Nature Biotechnol. 19:342 (2001). A variety of oligonucleotide array designs is suitable for the practice of this invention.
In one embodiment the one or more oligonucleotides include a plurality of oligonucleotides that each hybridize to a different gene expressed in a particular tissue type. For example, the tissue can be developing wood.
In one embodiment, a nucleic acid sample obtained from a plant can be amplified and, optionally labeled with a detectable label. Any method of nucleic acid amplification and any detectable label suitable for such purpose can be used. For example, amplification reactions can be performed using, e.g. Ambion's MessageAmp, which creates “antisense” RNA or “aRNA” (complementary in nucleic acid sequence to the RNA extracted from the sample tissue). The RNA can optionally be labeled using CyDye fluorescent labels. During the amplification step, aaUTP is incorporated into the resulting aRNA. The CyDye fluorescent labels are coupled to the aaUTPs in a non-enzymatic reaction. Subsequent to the amplification and labeling steps, labeled amplified antisense RNAs are precipitated and washed with appropriate buffer, and then assayed for purity. For example, purity can be assay using a NanoDrop spectrophotometer. The nucleic acid sample is then contacted with an oligonucleotide array having, attached to a solid substrate (a “microarray slide”), oligonucleotide sample probes capable of hybridizing to nucleic acids of interest which may be present in the sample. The step of contacting is performed under conditions where hybridization can occur between the nucleic acids of interest and the oligonucleotide probes present on the array. The array is then washed to remove non-specifically bound nucleic acids and the signals from the labeled molecules that remain hybridized to oligonucleotide probes on the solid substrate are detected. The step of detection can be accomplished using any method appropriate to the type of label used. For example, the step of detecting can accomplished using a laser scanner and detector. For example, on can use and Axon scanner which optionally uses GenePix Pro software to analyze the position of the signal on the microarray slide.
Data from one or more microarray slides can analyzed by any appropriate method known in the art.
Oligonucleotide probes used in the methods of the present invention, including microarray techniques, can be generated using PCR. PCR primers used in generating the probes are chosen, for example, based on the sequences of SEQ ID NOs: 1-252, 765 and 768, to result in amplification of unique fragments of the monolignol synthesis, monolignol transport, and lignin polymerization genes (i.e., fragments that hybridize to only one polynucleotide of any one of SEQ ID NOs: 1-252, 765 and 768 under standard hybridization conditions). Computer programs are useful in the design of primers with the required specificity and optimal hybridization properties. For example, Li and Stormo, supra, discuss a method of probe selection using ProbeSelect which selects an optimum oligonucleotide probe based on the entire gene sequence as well as other gene sequences to be probed at the same time.
In one embodiment, oligonucleotide control probes also are used. Exemplary control probes can fall into at least one of three categories referred to herein as (1) normalization controls, (2) expression level controls and (3) negative controls. In microarray methods, one or more of these control probes may be provided on the array with the inventive monolignol synthesis, monolignol transport, or lignin polymerization gene-related oligonucleotides.
Normalization controls correct for dye biases, tissue biases, dust, slide irregularities, malformed slide spots, etc. Normalization controls are oligonucleotide or other nucleic acid probes that are complementary to labeled reference oligonucleotides or other nucleic acid sequences that are added to the nucleic acid sample to be screened. The signals obtained from the normalization controls, after hybridization, provide a control for variations in hybridization conditions, label intensity, reading efficiency and other factors that can cause the signal of a perfect hybridization to vary between arrays. In one embodiment, signals (e.g., fluorescence intensity or radioactivity) read from all other probes used in the method are divided by the signal from the control probes, thereby normalizing the measurements.
Virtually any probe can serve as a normalization control. Hybridization efficiency varies, however, with base composition and probe length. Preferred normalization probes are selected to reflect the average length of the other probes being used, but they also can be selected to cover a range of lengths. Further, the normalization control(s) can be selected to reflect the average base composition of the other probes being used. In one embodiment, only one or a few normalization probes are used, and they are selected such that they hybridize well (i.e., without forming secondary structures) and do not match any test probes. In one embodiment, the normalization controls are mammalian genes.
Expression level control probes hybridize specifically with constitutively expressed genes present in the biological sample. Virtually any constitutively expressed gene provides a suitable target for expression level control probes. Typically, expression level control probes have sequences complementary to subsequences of constitutively expressed “housekeeping genes” including, but not limited to certain photosynthesis genes.
As used herein, “negative control” probes are not complementary to any of the test oligonucleotides (i.e., the inventive monolignol synthesis, monolignol transport, and lignin polymerization gene-related oligonucleotides), normalization controls, or expression controls. In one embodiment, the negative control is a mammalian gene which is not complementary to any other sequence in the sample.
The terms “background” and “background signal intensity” refer to hybridization signals resulting from non-specific binding or other interactions between the labeled target nucleic acids (i.e., mRNA present in the biological sample) and components of the oligonucleotide array. Background signals also can be produced by intrinsic fluorescence of the array components themselves.
A single background signal can be calculated for the entire array, or a different background signal can be calculated for each target nucleic acid. In a one embodiment, background is calculated as the average hybridization signal intensity for the lowest 5 to 10 percent of the oligonucleotide probes being used, or, where a different background signal is calculated for each target gene, for the lowest 5 to 10 percent of the probes for each gene. Where the oligonucleotide probes corresponding to a particular monolignol synthesis, monolignol transport, and lignin polymerization gene hybridize well and, hence, appear to bind specifically to a target sequence, they should not be used in a background signal calculation. Alternatively, background can be calculated as the average hybridization signal intensity produced by hybridization to probes that are not complementary to any sequence found in the sample (e.g., probes directed to nucleic acids of the opposite sense or to genes not found in the sample). In microarray methods, background can be calculated as the average signal intensity produced by regions of the array that lack any oligonucleotides probes at all.
3. PCR-Based Methods
In another embodiment, PCR-based methods are used to detect gene expression. These methods include reverse-transcriptase-mediated polymerase chain reaction (RT-PCR) including real-time and endpoint quantitative reverse-transcriptase-mediated polymerase chain reaction (Q-RTPCR). These methods are well known in the art. For example, methods of quantitative PCR can be carried out using kits and methods that are commercially available from, for example, Applied BioSystems and Stratagene®. See also Kochanowski, Q
Gene expression can also be observed in solution using Q-RTPCR. Q-RTPCR relies on detection of a fluorescent signal produced proportionally during amplification of a PCR product. See Innis et al., supra. Like the traditional PCR method, this technique employs PCR oligonucleotide primers, typically 15-30 bases long, that hybridize to opposite strands and regions flanking the DNA region of interest. Additionally, a probe (e.g., TaqMan®, Applied Biosystems) is designed to hybridize to the target sequence between the forward and reverse primers traditionally used in the PCR technique. The probe is labeled at the 5′ end with a reporter fluorophore, such as 6-carboxyfluorescein (6-FAM) and a quencher fluorophore like 6-carboxy-tetramethyl-rhodamine (TAMRA). As long as the probe is intact, fluorescent energy transfer occurs which results in the absorbance of the fluorescence emission of the reporter fluorophore by the quenching fluorophore. As Taq polymerase extends the primer, however, the intrinsic 5′ to 3′ nuclease activity of Taq degrades the probe, releasing the reporter fluorophore. The increase in the fluorescence signal detected during the amplification cycle is proportional to the amount of product generated in each cycle.
The forward and reverse amplification primers and internal hybridization probe is designed to hybridize specifically and uniquely with one nucleotide derived from the transcript of a target gene. In one embodiment, the selection criteria for primer and probe sequences incorporates constraints regarding nucleotide content and size to accommodate TaqMan® requirements.
SYBR Green® can be used as a probe-less Q-RTPCR alternative to the Taqman®-type assay, discussed above. ABI Prism® 7900 Sequence Detection System User Guide Applied Biosystems, chap. 1-8, App. A-F. (2002).
A device measures changes in fluorescence emission intensity during PCR amplification. The measurement is done in “real time,” that is, as the amplification product accumulates in the reaction. Other methods can be used to measure changes in fluorescence resulting from probe digestion. For example, fluorescence polarization can distinguish between large and small molecules based on molecular tumbling (see, e.g., U.S. Pat. No. 5,593,867).
4. Protein Detection Methods
Proteins can be observed by any means known in the art, including immunological methods, enzyme assays and protein array/proteomics techniques.
Measurement of the translational state can be performed according to several protein methods. For example, whole genome monitoring of protein—the “proteome”—can be carried out by constructing a microarray in which binding sites comprise immobilized, preferably monoclonal, antibodies specific to a plurality of proteins having an amino acid sequence of any of SEQ ID NOs: 253-504, 766 and 769 or proteins encoded by the genes of SEQ ID NOs: 1-252, 765 and 768 or conservative variants thereof. See Wildt et al., Nature Biotechnol. 18: 989 (2000). Methods for making polyclonal and monoclonal antibodies are well known, as described, for instance, in Harlow & Lane, A
Alternatively, proteins can be separated by two-dimensional gel electrophoresis systems. Two-dimensional gel electrophoresis is well-known in the art and typically involves isoelectric focusing along a first dimension followed by SDS-PAGE electrophoresis along a second dimension. See, e.g., Hames et al, G
C. Correlating Gene Expression to Phenotype and Tissue Development
As discussed above, the invention provides methods and tools to correlate gene expression to plant phenotype. Gene expression may be examined in a plant having a phenotype of interest and compared to a plant that does not have the phenotype or has a different phenotype. Such a phenotype includes, but is not limited to, increased drought tolerance, herbicide resistance, reduced or increased height, reduced or increased branching, enhanced cold and frost tolerance, improved vigor, enhanced color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced resistance of the wood to decay, enhanced resistance to fungal diseases, altered attractiveness to insect pests, increased disease tolerance, increased insect tolerance, increased water-stress tolerance, improved texture, increased germination, increased micronutrient uptake, production of novel resins, increased or decreased cellulose content, increased or decreased lignin content, increased or decreased nonlignin cell wall phenolics and production of novel proteins or peptides.
In another embodiment, the phenotype includes one or more of the following traits: propensity to form reaction wood, a reduced period of juvenility, an increased period of juvenility, self-abscising branches, accelerated reproductive development or delayed reproductive development.
In a further embodiment, the phenotype that is differs in the plants compares includes one or more of the following: lignin quality, lignin structure, wood composition, wood appearance, wood density, wood strength, wood stiffness, cellulose polymerization, fiber dimensions, lumen size, proportion of rays, proportion of vessel elements, other plant components, plant cell division, plant cell development, number of cells per unit area, cell size, cell shape, cell wall composition, proportion of nonlignin cell wall phenolics, rate of wood formation, aesthetic appearance of wood, formation of stem defects, average microfibril angle, width of the S2 cell wall layer, rate of growth, rate of root formation ratio of root to branch vegetative development, leaf area index, and leaf shape. Phenotype can be assessed by any suitable means as discussed above, such as, for example Hertzberg, supra, Ye and Sundström, supra, U.S. Patent Application Publication Nos. 2002/0107644 and 2002/0113212, Marita et al., supra.
It will be apparent to those skilled in the art that various modifications and variations can be made in the methods and compositions of the present invention without departing from the spirit or scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.
The following examples are given to illustrate the present invention. It should be understood, however, that the invention is not to be limited to the specific conditions or details described in these examples. Throughout the specification, any and all references to a publicly available document, including a U.S. patent, are specifically incorporated by reference in their entirety.
Example 1 demonstrates how monolignol synthesis, monolignol transport, and lignin polymerization and monolignol synthesis, monolignol transport, and lignin polymerization-like genes are isolated and characterized in E. grandis and P. radiata.
Total RNA was extracted from plant tissue (using the protocol of Chang et al., Plant Mol. Biol. Rep. 11:113-116 (1993). Plant tissue samples were obtained from phloem (P), cambium (C), expanding xylem (X1), and differentiating and lignifying xylem (X2).
mRNA was isolated from the total RNA preparation using either a Poly(A) Quik mRNA Isolation Kit (Stratagene, La Jolla, Calif.) or Dynal Beads Oligo (dT)25 (Dynal, Skogen, Norway). cDNA expression libraries were constructed from the purified mRNA by reverse transcriptase synthesis followed by insertion of the resulting cDNA clones in Lambda ZAP using a ZAP Express cDNA Synthesis Kit (Stratagene), according to the using the manufacturer's protocol. The resulting cDNAs were packaged using a Gigapack II Packaging Extract (Stratagene) using an aliquot (1-5 μL) from the 5 μL ligation reaction dependent upon the library. Mass excision of the library was done using XL1-Blue MRF' cells and XLOLR cells (Stratagene) with ExAssist helper phage (Stratagene). The excised phagemids were diluted with NZY broth (Gibco BRL, Gaithersburg, Md.) and plated out onto LB-kanamycin agar plates containing X-gal and isopropylthio-beta-galactoside (IPTG).
Of the colonies plated and selected for DNA miniprep, 99% contained an insert suitable for sequencing. Positive colonies were cultured in NZY broth with kanamycin and cDNA was purified by means of alkaline lysis and polyethylene glycol (PEG) precipitation. Agarose gel at 1% was used to screen sequencing templates for chromosomal contamination. Dye primer sequences were prepared using a Turbo Catalyst 800 machine (Perkin Elmer/Applied Biosystems Division, Foster City, Calif.) according to the manufacturer's protocol.
DNA sequence for positive clones was obtained using a Perkin Elmer/Applied Biosystems Division Prism 377 sequencer. cDNA clones were sequenced first from the 5′ end and, in some cases, also from the 3′ end. For some clones, internal sequence was obtained using either Exonuclease III deletion analysis, yielding a library of differentially sized subclones in pBK-CMV, or by direct sequencing using gene-specific primers designed to identify regions of the gene of interest. The determined cDNA sequences are provided in SEQ ID NOS: 1-252, 765 and 768. The predicted polypeptide sequences are SEQ ID NOs: 253-504, 766 and 769.
To identify monolignol synthesis, monolignol transport, and lignin polymerization gene candidates in P. radiata and E. grandis databases, the cDNA sequences were compared to public domain sequences (by SWISS-PROT/TrEMBL ID's) to search against the pine and eucalyptus databases (non-redundant by contig, expect<1.0e−2).
The contig consensus DNA and protein sequences were then obtained for these hits, and duplicate sequences were identified. A multiple alignment was then carried out with the protein sequences. The protein alignment was created using the remaining pine and eucalyptus sequences along with the Arabidopsis members. From the protein alignment, a dendogram was created. These sequences were analyzed by primer walking to provide a full length sequence (best HT pick from the contig analyzed for full length sequence).
The public domain monolignol synthesis, monolignol transport, and lignin polymerization gene sequences from maize, cotton, rice, and poplar were also extracted and blasted against the pine and eucalyptus databases. The completed primer walked pine and eucalyptus sequences were also blasted against ownseq and the top 500 hits were taken. This was done so that the sequences could be used to search further and ensure that nothing in the pine and eucalyptus databases had been missed by using the Arabidopsis superfamily. This search resulted in an additional 4 sequences which were not found in the previous searches. These sequences were then also sent for primer walked full length sequence.
After removing a small number of additional duplicates after primer walking, pine and eucalyptus primer walked monolignol synthesis, monolignol transport, and lignin polymerization superfamily members were identified. The classification of these sequences was confirmed by alignment with ClustalX, the corresponding dendogram, and MEME/MAST analysis.
To identify additional sequence 5′ or 3′ of a partial cDNA sequence in a cDNA library, 5′ and 3′ rapid amplification of cDNA ends (RACE) was performed. using the SMART RACE cDNA amplification kit (Clontech Laboratories, Palo Alto, Calif.). Generally, the method entailed first isolating poly(A) mRNA, performing first and second strand cDNA synthesis to generate double stranded cDNA, blunting cDNA ends, and then ligating of the SMART RACE Adaptor to the cDNA to form a library of adaptor-ligated ds cDNA. Gene-specific primers were designed to be used along with adaptor specific primers for both 5′ and 3′ RACE reactions. Using 5′ and 3′ RACE reactions, 5′ and 3′ RACE fragments were obtained, sequenced, and cloned. The process may be repeated until 5′ and 3′ ends of the full-length gene were identified. A full-length cDNA may generated by PCR using primers specific to 5′ and 3′ ends of the gene by end-to-end PCR.
For example, to amplify the missing 5′ region of a gene from first-strand cDNA, a primer was designed 5′→3′ from the opposite strand of the template sequence, and from the region between ˜100-200 bp of the template sequence. A successful amplification should give an overlap of ˜100 bp of DNA sequence between the 5′ end of the template and PCR product.
RNA was extracted from four pine tissues, namely seedling, xylem, phloem and structural root using the Concert Reagent Protocol (Invitrogen, Carlsbad, Calif.) and standard isolation and extraction procedures. The resulting RNA was then treated with DNase, using 10 U/μl DNase I (Roche Diagnostics, Basel, Switzerland). For 100 μg of RNA, 9 μl 10× DNase buffer (Invitrogen, Carlsbad, Calif.), 10 μl of Roche DNase I and 90 μl of Rnase-free water was used. The RNA was then incubated at room temperature for 15 minutes and 1/10 volume 25 mM EDTA is added. A RNeasy mini kit (Qiagen, Venlo, The Netherlands) was used for RNA purification according to manufacturer's protocol.
To synthesize cDNA, the extracted RNA from xylem, phloem, seedling and root was used and the SMART RACE cDNA amplification kit (Clontech Laboratories Inc, Palo Alto, Calif.) was followed according to manufacturer's protocol. For the RACE PCR, the cDNA from the four tissue types was combined. The master mix for PCR was created by combining equal volumes of cDNA from xylem, phloem, root and seedling tissues. PCR reactions were performed in 96 well PCR plates, with 1 μl of primer from primer dilution plate (10 mM) to corresponding well positions. 49 μl of master mix is aliquoted into the PCR plate with primers. Thermal cycling commenced on a GeneAmp 9700 (Applied Biosystems, Foster City, Calif.) at the following parameters:
94° C. (5 sec),
72° C. (3 min), 5 cycles;
94° C. (5 sec),
70° C. (10 sec),
72° C. (3 min), 5 cycles;
94° C. (5 sec),
68° C. (10 sec),
72° C. (3 min), 25 cycles.
cDNA was separated on an agarose gel following standard procedures. Gel fragments were excised and eluted from the gel by using the Qiagen 96-well Gel Elution kit, following the manufacturer's instructions.
PCR products were ligated into pGEMTeasy (Promega, Madison, Wis.) in a 96 well plate overnight according to the following specifications: 60-80 ng of DNA, 5 μl 2× rapid ligation buffer, 0.5 μl pGEMT easy vector, 0.1 μl DNA ligase, filled to 10 μl with water, and incubated overnight.
Each clone was transformed into E. coli following standard procedures and DNA was extracted from 12 clones picked by following standard protocols. DNA extraction and the DNA quality was verified on an 1 agarose gel. The presence of the correct size insert in each of the clones was determined by restriction digests, using the restriction endonuclease EcoRI, and gel electrophoresis, following standard laboratory procedures.
Example 3 illustrates a procedure for RNA extraction and purification, which is particularly useful for RNA obtained from conifer needle, xylem, cambium, and phloem.
Tissue is obtained from conifer needle, xylem, cambium or phloem. The tissue is frozen in liquid nitrogen and ground. The total RNA is extracted using Concert Plant RNA reagent (Invitrogen). The resulting RNA sample is extracted into phenol:chloroform and treated with DNase. The RNA is then incubated at 65° C. for 2 minutes followed by centrifugation at 4° C. for 30 minutes. Following centrifugation, the RNA is extracted into phenol at least 10 times to remove contaminants.
The RNA is further cleaned using RNeasy columns (Qiagen). The purified RNA is quantified using RiboGreen reagent (Molecular Probes) and purity assessed by gel electrophoresis.
RNA is then amplified using MessageAmp (Ambion). Aminoallyl-UTP and free UTP are added to the in vitro transcription of the purified RNA at a ratio of 4:1 aminoallyl-UTP-to-UTP. The aminoallyl-UTP is incorporated into the new RNA strand as it is transcribed. The amino-allyl group is then reacted with Cy dyes to attach the colorimetric label to the resulting amplified RNA using the Amersham procedure modified for use with RNA. Unincorporated dye is removed by ethanol precipitation. The labeled RNA is quantified spectrophotometrically (NanoDrop). The labeled RNA is fragmented by heating to 95° C. as described in Hughes et al., Nature Biotechnol. 19:342 (2001).
Example 4 illustrates how monolignol synthesis, monolignol transport, and lignin polymerization genes important for wood development in P. radiata are determined and how oligonucleotides which uniquely bind to those genes can be designed and synthesized for use on a microarray.
Pine trees of the species P. radiata are grown under natural light conditions. Tissue samples are prepared as described in, e.g., Sterky et al., Proc. Nat'l Acad. Sci. 95:13330 (1998). Specifically, tissue samples are collected from woody trees having a height of 5 meters. Tissue samples of the woody trees are prepared by taking tangential sections through the cambial region of the stem. The stems are sectioned horizontally into sections ranging from juvenile (top) to mature (bottom). The stem sections separated by stage of development are further separated into 5 layers by peeling into sections of phloem, differentiating phloem, cambium, differentiating xylem, developing xylem, and mature xylem. Tissue samples, including leaves, buds, shoots, and roots are also prepared from seedlings of the species P. radiata.
RNA is isolated and ESTs generated as described in Example 1 or Sterky et al., supra. The nucleic acid sequences of ESTs derived from samples containing developing wood are compared with nucleic acid sequences of genes known to be involved in monolignol synthesis, monolignol transport, or lignin polymerization. ESTs from samples that do not contain developing wood are also compared with sequences of genes known to be involved in the plant cell cycle. An in silico hybridization analysis is performed using BLAST (NCBI). TABLES 9 and 10 show in silico hybridization data for monolignol synthesis, monolignol transporation, and lignin polymerization proteins in P. radiata (TABLE 9) and E. grandis (TABLE 10).
Sequences from among the known monolignol synthesis, monolignol transport, and lignin polymerization genes that show hybridization in silico to ESTs made from samples containing developing wood, but that do not hybridize to ESTs from samples not containing developing wood are selected for further examination.
cDNA clones containing sequences that hybridize to the genes showing wood-preferred expression are selected from cDNA libraries using techniques well known in the art of molecular biology. Using the sequence information, oligonucleotides are designed such that each oligonucleotide is specific for only one cDNA sequence in the library. The oligonucleotide sequences are provided in TABLE 4 and TABLE 8. 60-mer oligonucleotide probes are designed using the method of Li and Stormo, supra, or using software such as ArrayDesigner, GeneScan, and ProbeSelect.
The oligonucleotides are then synthesized in situ described in Hughes et al., Nature Biotechnol. 19:324 (2002) or as described in Kane et al., Nucleic Acids Res. 28:4552 (2000) and affixed to an activated glass slide (Sigma-Genosis, The Woodlands, Tex.) using a 5′ amino linker. The position of each oligonucleotide on the slide is known.
Example 5 illustrates how RNAs of tissues from multiple pine species, in this case both P. radiata and loblolly pine P. taeda trees, are selected for analysis of the pattern of gene expression associated with wood development in the juvenile wood and mature wood forming sections of the trees using the microarrays derived from P. radiata cDNA sequences described in Example 4.
Open pollinated trees of approximately 16 years of age are selected from plantation-grown sites, in the United States for loblolly pine, and in New Zealand for radiata pine. Trees are felled during the spring and summer seasons to compare the expression of genes associated with these different developmental stages of wood formation. Trees are felled individually and trunk sections are removed from the bottom area approximately one to two meters from the base and within one to two meters below the live crown. The section removed from the basal end of the trunk contains mature wood. The section removed from below the live crown contains juvenile wood. Samples collected during the spring season are termed earlywood or springwood, while samples collected during the summer season are considered latewood or summerwood. Larson et al., Gen. Tech. Rep. FPL-GTR-129. Madison, Wis.: U.S. Department of Agriculture, Forest Service, Forest Products Laboratory. p. 42.
Tissues are isolated from the trunk sections such that phloem, cambium, developing xylem, and maturing xylem are removed. These tissues are collected only from the current year's growth ring. Upon tissue removal in each case, the material is immediately plunged into liquid nitrogen to preserve the nucleic acids and other components. The bark is peeled from the section and phloem tissue removed from the inner face of the bark by scraping with a razor blade. Cambium tissue is isolated from the outer face of the peeled section by gentle scraping of the surface. Developing xylem and lignifying xylem are isolated by sequentially performing more vigorous scraping of the remaining tissue. Tissues are transferred from liquid nitrogen into containers for long term storage at −70° C. until RNA extraction and subsequent analysis is performed.
Using these techniques and the microarrays as described in Example 4, a Caffeoyl-CoA O-methyltransferase (CCoAOMT) gene (SEQ ID NO: 80), was shown to be significantly up-regulated in steady state RNA levels detected in cambium and early and later developing xylem relative to phloem.
Example 6 illustrates procedures alternative to those used in Example 3 for RNA extraction and purification, particularly useful for RNA obtained from a variety of tissues of woody plants, and a procedure for hybridization and data analysis using the arrays described in Example 4.
RNA was isolated according to the protocol of Chang et al., Plant Mol. Biol. Rep. 11:113. DNA is removed using DNase I (Invitrogen, Carlsbad, Calif.) according to the manufacturer's recommendations. The integrity of the RNA samples was determined using the Agilent 2100 Bioanalyzer (Agilent Technologies, USA).
10 μg of total RNA from each tissue was reversed transcribed into cDNA using known methods.
In the case of Pinus radiata phloem tissue, it can be difficult to extract sufficient amounts of total RNA for normal labelling procedures. Total RNA was extracted and treated as previously described and 100 ng of total RNA is amplified using the Ovation™ Nanosample RNA Amplification system from NuGEN™ (NuGEN, CA, USA). Similar amplification kits such as those manufactured by Ambion may alternatively be used. The amplified RNA was reverse transcribed into cDNA and labelled as described above.
Hybridization and stringency washes are performed using the protocol as described in the US patent application for “Methods and Kits for Labeling and Hybridizing cDNA for Microarray Analysis” (supra) at 42 C. The arrays (slides) are scanned using a ScanArray 4000 Microarray Analysis System (GSI Lumonics, Ottawa, ON, Canada). Raw, non-normalized intensity values are generated using QUANTARRAY software (GSI Lumonics, Ottawa, ON, Canada).
A fully balanced, incomplete block experimental design (Kerr and Churchill, Gen. Res. 123:123 (2001)) was used in order to design an array experiment that would allow maximum statistical inferences from analyzed data.
Gene expression data was analyzed using the SAS® Microarray Solution software package (The SAS Institute, Cary, N.C., USA). Resulting data was then visualized using JMP® (The SAS Institute, Cary, N.C., USA).
Analysis done for this experiment was an ANOVA approach with mixed model specification (Wolfinger et al., J. Comp. Biol. 8:625-637). Two steps of linear mixed models were applied. The first one, normalization model, was applied for global normalization at slide-level. The second one, gene model, was applied for doing rigorous statistical inference on each gene. Both models are stated in Models (1) and (2).
log2(Yijkls)=θij+Dk+Sl+DSkl+ωijkls (1)
Rijkls(g)=μij(g)+Dk(g)+Sl(g)+DSkl(g)+SSls(g)+εijkls(g) (2)
Yijkls represents the intensity of the sth spot in the lth slide with the kth dye applying the jth treatment for the ith cell line. θij, Dk, Sl, and DSkl represent the mean effect of the jth treatment in the ith cell line, the kth dye effect, the lth slide random effect, and the random interaction effect of the kth dye in the lth slide. ωijkls is the stochastic error term. represent the similar roles as θij, Dk, Sl, and DSkl except they are specific for the gth gene. Rijkls(g) represents the residual of the gth gene from model (1). μij(g), Dk(g), Sl(g), and DSkl(g) represent the similar roles as θij, Dk, Sl, and DSkl except they are specific for the gth gene. SSls(g) represent the spot by slide random effect for the gth gene. εijkls(g) represent the stochastic error term. All random terms are assumed to be normal distributed and mutually independent within each model.
According to the analysis described above, certain cDNAs, as prepented in TABLE 11, were found to be differentially expressed. In TABLE 11, the cDNAs are listed in from greatest to least fold-change of expression in later developing xylem relative to cambium. In addition SEQ ID NO: 57, a putative p-courmarate 3-monooxygenase cDNA, was identified as being expressed in phloem tissue to a greater degree than in cambium tissue.
TABLE 11
SEQ ID NO
Putative Gene
Comment
41
Laccase
more expression in xylem than in
cambium
44
Laccase
more expression in xylem than in
cambium
50
Laccase
more expression in xylem than in
cambium
63
Trans-cinnamate
appears to be expressed only in later
4-monooxygenase
developing xylem
52
Laccase
more expression in xylem than in
cambium
105
Peroxidase
more expression in xylem than in
cambium
51
Laccase
more expression in xylem than in
cambium
52
Laccase
appears to be expressed only in later
developing xylem
10
Cinnamoyl-CoA
more expression in xylem than in
reductase
cambium
94
Peroxidase
less expression in xylem than in
cambium
The involvement of these specific genes in wood development was inferred through the association of the up-regulation or down-regulation of genes to the particular stages of wood development. Both the spatial continuum of wood development across a section (phloem, cambium, developing xylem, maturing xylem) at a particular season and tree trunk position and the relationships of season and tree trunk position were considered when making associations of gene expression to the relevance in wood development.
Example 7 demonstrates how one can correlate monolignol synthesis, monolignol transport, and lignin polymerization gene expression with agronomically important wood phenotypes such as density, stiffness, strength, distance between branches, and spiral grain.
Mature clonally propagated pine trees are selected from among the progeny of known parent trees for superior growth characteristics and resistance to important fungal diseases. The bark is removed from a tangential section and the trees are examined for average wood density in the fifth annual ring at breast height, stiffness and strength of the wood, and spiral grain. The trees are also characterized by their height, mean distance between major branches, crown size, and forking.
To obtain seedling families that are segregating for major genes that affect density, stiffness, strength, distance between branches, spiral grain and other characteristics that may be linked to any of the genes affecting these characteristics, trees lacking common parents are chosen for specific crosses on the criterion that they exhibit the widest variation from each other with respect to the density, stiffness, strength, distance between branches, and spiral grain criteria. Thus, pollen from a tree exhibiting high density, low mean distance between major branches, and high spiral grain is used to pollinate cones from the unrelated plus tree among the selections exhibiting the lowest density, highest mean distance between major branches, and lowest spiral grain. It is useful to note that “plus trees” are crossed such that pollen from a plus tree exhibiting high density are used to pollinate developing cones from another plus tree exhibiting high density, for example, and pollen from a tree exhibiting low mean distance between major branches would be used to pollinate developing cones from another plus tree exhibiting low mean distance between major branches.
Seeds are collected from these controlled pollinations and grown such that the parental identity is maintained for each seed and used for vegetative propagation such that each genotype is represented by multiple ramets. Vegetative propagation is accomplished using micropropagation, hedging, or fascicle cuttings. Some ramets of each genotype are stored while vegetative propagules of each genotype are grown to sufficient size for establishment of a field planting. The genotypes are arrayed in a replicated design and grown under field conditions where the daily temperature and rainfall are measured and recorded.
The trees are measured at various ages to determine the expression and segregation of density, stiffness, strength, distance between branches, spiral grain, and any other observable characteristics that may be linked to any of the genes affecting these characteristics. Samples are harvested for characterization of cellulose content, lignin content, cellulose microfibril angle, density, strength, stiffness, tracheid morphology, ring width, and the like. Certain genotypes are selected from the population on the basis that they exhibit extremes in density, as measured in ring 5 of an increment core, or in stiffness (modulus of elasticity) as measured by means of a nondestructive stress wave instrument. An example of such an instrument is described in Wang et al., Experimental Techniques 191:27-29 (2000).
Those skilled in the art of tree mensuration will recognize that any of a number of such techniques are available and suitable for making such selections. The genotypes that are selected as representing the extremes are then further selected in order to find paired samples of genotypes, one in the highest quartile andone in the lowest quartile for each trait, for which all replicate trees in the field are approximately the same size and are healthy and lack evidence of herbivory, so that health and size effects are not confounded with wood quality traits in the microarray analysis. RNA samples are then isolated from scrapings taken from these trees in early spring and late summer as described in Example 5, and assayed using an oligo microarray as described in Example 6.
Example 8 demonstrates how responses to environmental conditions such as light and season alter plant phenotype and can be correlated to monolignol synthesis, monolignol transport, and lignin polymerization gene expression using microarrays. In particular, the changes in gene expression associated with wood density are examined.
Trees of three different clonally propagated E. grandis hybrid genotypes are grown on a site with a weather station that measures daily temperatures and rainfall. During the spring and subsequent summer, genetically identical ramets of the three different genotypes are first photographed with north-south orientation marks, using photography at sufficient resolution to show bark characteristics of juvenile and mature portions of the plant, and then felled. The age of the trees is determined by planting records and confirmed by a count of the annual rings. In each of these trees, mature wood is defined as the outermost rings of the tree below breast height, and juvenile wood as the innermost rings of the tree above breast height. Each tree is accordingly sectored as follows:
NM—NORTHSIDE MATURE
SM—SOUTHSIDE MATURE
NT—NORTHSIDE TRANSITION
ST—SOUTHSIDE TRANSITION
NJ—NORTHSIDE JUVENILE
SJ—SOUTHSIDE JUVENILE
Tissue is harvested from the plant trunk as well as from juvenile and mature form leaves. Samples are prepared simultaneously for phenotype analysis, including plant morphology and biochemical characteristics, and gene expression analysis. The height and diameter of the tree at the point from which each sector was taken is recorded, and a soil sample from the base of the tree is taken for chemical assay. Samples prepared for gene expression analysis are weighed and placed into liquid nitrogen for subsequent preparation of RNA samples for use in the microarray experiment. The tissues are denoted as follows:
Thin slices in tangential and radial sections from each of the sectors of the trunk are fixed as described in Ruzin, P
For biochemical analysis, 50 grams from each of the harvest samples are freeze-dried and analyzed, using biochemical assays well known to those skilled in the art of plant biochemistry for quantities of simple sugars, amino acids, lipids, other extractives, lignin, and cellulose. See, e.g., Pettersen & Schwandt, J. Wood Chem. & Technol. 11:495 (1991).
In the present example, the phenotypes chosen for comparison are high density wood, average density wood, and low density wood. Nucleic acid samples are prepared as described in Example 3, from trees harvested in the spring and summer. Gene expression profiling by hybridization and data analysis is performed as described above.
Using similar techniques and clonally propagated individuals one can examine monolignol synthesis, monolignol transport, and lignin polymerization gene expression as it is related to other complex wood characteristics such as strength, stiffness and spirality.
Example 9 demonstrates how a monolignol synthesis, monolignol transport, and lignin polymerization gene can be linked to a tissue-preferred promoter and expressed in pine resulting in a plant with increased wood density.
A monolignol synthesis, monolignol transport, and lignin polymerization gene, which is more highly expressed during the early spring, is identified by the method described in Example 7. A DNA construct having the density-related polypeptide operably linked to a xylem-preferred promoter is placed into an appropriate binary vector and transformed into pine using the methods described herein. Pine plants are transformed as described in herein and the transgenic pine plants are used to establish a forest planting. Increased density even in the spring wood (early wood) is observed in the transgenic pine plants relative to control pine plants which are not transformed with the density related DNA construct.
Using techniques well known to those skilled in the art of molecular biology, the sequence of the monolignol synthesis, monolignol transport, or lignin polymerization gene isolated in Example 2 is analyzed in genomic DNA isolated from alfalfa. This enables the identification of an orthologue in alfalfa whose sequence is then used to create an RNAi knockout construct. This construct is then transformed into alfalfa. See, e.g., Austin et al., Euphytica 85, 381 (1995). The regenerated transgenic plants show lower fiber content and increased ray cell content in the xylem. Such properties improve digestability which results in higher growth rates in cattle fed on this alfalfa as compared to wild-type alfalfa of the same species.
Example 11 demonstrates how gene expression analysis can be used to find gene variants which are present in mature plants having a desirable phenotype. The presence or absence of such a variant can be used to predict the phenotype of a mature plant, allowing screening of the plants at the seedling stage. Although this example employs eucalyptus, the method used herein is also useful in breeding programs for pine and other tree species.
The sequence of a putative density-related gene is used to probe genomic DNA isolated from Eucalyptus that vary in density as described in previous examples. Non-transgenically produced Eucalyptus hybrids of different wood phenotypes are examined. One hybrid exhibits high wood density and another hybrid exhibits lower wood density. A molecular marker in the 3′ portion of the coding region is found which distinguishes a high-density gene variant from a lower density gene variant.
This molecular marker enables tree breeders to assay non-transgenic Eucalyptus hybrids for likely density profiles while the trees are still at seedling stage, whereas in the absence of the marker, tree breeders must wait until the trees have grown for multiple years before density at harvest age can be reliably predicted. This enables selective outplanting of the best trees at seedling stage rather than an expensive culling operation and resultant erosion at thinning age. This molecular marker is further useful in the breeding program to determine which parents will give rise to high density outcross progeny.
Molecular markers found in the 3′ portion of the coding region of the gene that do not correspond to variants seen more frequently in higher or lower wood density non-transgenic Eucalyptus hybrid trees are also useful. These markers are found to be useful for fingerprinting different genotypes of Eucalyptus, for use in identity-tracking in the breeding program and in plantations.
Example 12 describes microarrays for identifying gene expression differences that contribute to the phenotypic characteristics that are important in commercial wood, namely wood appearance, stiffness, strength, density, fiber dimensions, coarseness, cellulose and lignin content, lignin composition, extractives content and the like.
Woody trees of genera that produce commercially important wood products, in this case Pinus and Eucalyptus, are felled from various sites and at various times of year for the collection and isolation of RNA from developing xylem, cambium, phloem, leaves, buds, roots, and other tissues. RNA is also isolated from seedlings of the same genera.
All contigs are compared to both the ESTs made from RNA isolated from samples containing developing wood and the sequences of the ESTs made from RNA of various tissues that do not contain developing wood. Contigs containing primarily ESTs that show more hybridization in silico to ESTs made from RNA isolated from samples containing developing wood than to ESTs made from RNA isolated from samples not containing developing wood are determined to correspond to possible novel genes particularly expressed in developing wood. These contigs are then used for BLAST searches against public domain sequences. Those contigs that hybridize in silico with high stringency to no known genes or genes annotated as having only a “hypothetical protein” are selected for the next step. These contigs are considered putative novel genes showing wood-preferred expression.
The longest cDNA clones containing sequences hybridizing to the putative novel genes showing wood-preferred expression are selected from cDNA libraries using techniques well known to those skilled in the art of molecular biology. The cDNAs are sequenced and full-length gene-coding sequences together with untranslated flanking sequences are obtained where possible. Stretches of 45-80 nucleotides (or oligonucleotides) are selected from each of the sequences of putative novel genes showing wood-preferred expression such that each oligonucleotide probe hybridizes at high stringency to only one sequence represented in the ESTs made from RNA isolated from trees or seedlings of the same genus.
Oligomers are then chemically synthesized and placed onto a microarray slide as described in Example 4. Each oligomer corresponds to a particular sequence of a putative novel gene showing wood-preferred expression and to no other gene whose sequence is represented among the ESTs made from RNA isolated from trees or seedlings of the same genus.
Sample preparation and hybridization are carried out as in Example 4. The technique used in this example is more effective than use of a microarray using cDNA probes because the presence of a signal represents significant evidence of the expression of a particular gene, rather than of any of a number of genes that may contain similarities to the cDNA due to conserved functional domains or common evolutionary history. Thus, it is possible to differentiate homologous genes, such as those in the same family, but which may have different functions in phenotype determination.
This hybridization data, gained using the method of Example 6, enables the user to identify which of the putative novel genes actually possesses a pattern of coordinate expression with known genes, a pattern of expression consistent with a particular developmental role, and/or a pattern of expression that suggests that the gene has a promoter that drives expression in a valuable way.
The hybridization data obtained using this method can be used, for example, to identify a putative novel gene that shows an expression pattern particular to the tracheids with the lowest cellulose microfibril angle in developing spring wood (early wood). The promoter of this gene can also be isolated as in Example 8, and operably linked to a gene that has been shown as in Example 9 to be associated with late wood (summer wood). Transgenic pine plants containing this construct are generated using the methods of Example 9, and the early wood of these plants is then shown to display several characteristics of late wood, such as higher microfibril angle, higher density, smaller average lumen size, etc.
Example 13 demonstrates the use of a xylem-specific promoter functionally linked to a monolignol synthesis, monolignol transport, and lignin polymerization gene for increased plant biomass.
Xylem-specific monolignol synthesis, monolignol transport, and lignin polymerization gene transcripts are identified via array analyses of different secondary vasculature layers as described in Example 6. Candidate promoters linked to the genes corresponding to these transcripts are cloned from pine genomic DNA using, e.g., the BD Clontech GenomeWalker kit and tested in transgenic tobacco via a reporter assay(s) for cambium specificity/preference. The xylem-specific promoter overexpressing a monolignol synthesis, monolignol transport, and lignin polymerization gene gene involved is used to increase wood biomass. A tandem xylem-specific promoter is constructed driving the monolignol synthesis, monolignol transport, or lignin polymerization gene synthesis gene ORF. Boosted transcript levels of the candidate monolignol synthesis, monolignol transport, or lignin polymerization gene result in an increased xylem biomass phenotype.
Example 14 demonstrates the construction of a DNA contruct for use in expressing the monolignol synthesis, monolignol transport, and lignin polymerization genes in Pinus.
A backbone vector is prepared by adding additional restriction endonuclease sites to the mulitiple cloning site of the plasmid pBluescript (BRL Gibco Life Technologies, Gaithersburg Md.). The NotI and SstI sites in the original pBluescript vector are destroyed by digestion of the plasmid with NotI and SstI and filling in the ends using Klenow and T4 Polymerase (Invitrogen Corp., Carlsbad Calif.). The plasmid is circularized by blunt-end ligation and then digested with the restriction endonucleases EcoRI and HindIII to enable cloning of linkers. Linkers (phosphorylated at the 5′ end) containing additional restriction sites are annealed together and ligated into the EcoRI/HindIII-digested pBluescript vector. Unless otherwise noted, DNA constructs, primers useful for preparing such constructs and elements included in such constructs are depicted in TABLE 12.
The 3′ UTR from the P. radiata superubiquitin gene (U.S. Pat. No. 6,380,459) is cloned into the plasmid pBI-121 (See Jefferson et al., EMBO J. 6:3901-3907 (1987)). First, a fragment of the 3′ UTR of the gene is amplified using standard PCR techniques. These primers can contain additional nucleotides and, in this case, can contain an SstI restriction site for cloning into SstI-digested plasmid pBI-121. Then, the 3′ UTR fragment, containing the nos terminator, is transferred to the pBluescript plasmid. The 3′ UTR and nos terminator fragment of pBI-121 is amplified with PCR, cleaved with KpnI and ClaI and cloned into the modified pBluescript digested with KpnI and ClaI.
To this construct, the P. radiata superubiquitin promoter sequence with intron is added. The promoter/intron sequence is first amplified from the P. radiata superubiquitin sequence identifed in U.S. Pat. No. 6,380,459 (denoted therein as SEQ ID NO: 2) using standard PCR techniques. The amplified fragment is then ligated into the base vector using XbaI and PstI restriction digestion.
The P. radiata 4CL intron sequence from the P. radiata cDNA is amplified using standard PCR, then cloned into XcmI-digested vector backbone using T-tailed ligation.
A fragment from a P. radiata 4CL cDNA clone is amplified using standard PCR techniques (fragments A to G are depicted in SEQ ID NO: 789-795). Portions of the P. radiata 4CL cDNA clone were disclosed in U.S. Pat. Nos. 6,410,718 and 5,850,020. The primers are designed to add PstI and ClaI restriction sites to both ends of the amplified fragments. To clone the P. radiata 4CL fragment in the sense orientation, the amplified fragment is cut with the restriction enzyme PstI, blunt ended using Klenow and cloned into the backbone vector in a blunt-ended ClaI site. To clone the P. radiata 4CL fragment in the antisense orientation, the amplified fragment is digested with PstI and cloned into the PstI-digested backbone vector.
The complete RNAi cassette containing the promoter::sense fragment::intron::antisense fragment::3′UTR::nos terminator construct, is removed from the pBluescript plasmid by a NotI restriction digestion, and cloned into the binary vector pART29 (digested with NotI) using standard cloning techniques. The resulting DNA construct is labeled pARB513. The binary vector pART29 is a modified pART27 vector (Gleave et al., Plant Mol. Biol. 20:1203-1207 (1992)) that lacks the lacZ sequences and contains the Arabidopsis thaliana ubiquitin 3 (UBQ3) promoter in place of the nos 5′ promoter.
The pWVK147 vector is a pBI121 vector (Clontech laboratories, Palo Alto Calif.) with the 35S promoter GUS sequence removed and the nos promoter replaced with the UBQ10 promoter from Arabidopsis (Sun et a;. Plant J. 11:101-111 (1997)) operably linked to the nptII gene. A unique HpaI restriction site was added to pBI121 by the addition of an adapter ligated at the ApaI and KpnI sites.
The DNA constructs listed in TABLE 13 are assembled as described above but with modifications in at least one of the following: gene sequences; the promoter, and/or the binary vector.
To clone a different promoter as listed in TABLE 13 into the final vector, the P. radiata superubiquitin promoter intron vector is digested with SmaI and SstI restriction enzymes and using standard techniques. This fragment is cloned into a Bluescript vector containing either a 4CL promoter from P. taeda, an COMT promoter from Eucalyptus grandis, or a LIM promoter from P. radiata. The P. taeda 4CL promoter (U.S. Pat. No. 6,252,135 denoted therein as SEQ ID NO: 11), the E. grandis COMT promoter (as described in Example 1 of U.S. patent publication No. 20040146904), and the P. radiata LIM promoter (U.S. Patent publication No. 20040163146) are cloned with a similar strategy to the assembly of the P. radiata superubiquitin promoter sequence with intron and as described above. The complete RNAi cassette containing the promoter::sense fragment::intron::antisense fragment::3′UTR::nos terminator construct, is removed from the pBluescript plasmid by a NotI restriction digestion, and cloned into the binary vector pART29 or pWVK147 (digested with NotI).
TABLE 13
Final
Binary
Vector
Vector
Promoter
pARB553
pWVK147
Pinus radiata SuperUbiq + Intron (U.S. Pat.
No. 6,380,459)
pARB555
pWVK147
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
pARB561
pWVK147
Eucalyptus grandis COMT (U.S. Pat.
Publication No. 20040146904)
pARB562
pWVK147
Pinus radiata LIM (U.S. Pat. publication No.
20040163146)
pARB515
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
pARB534
pART29
Pinus radiata LIM (U.S. Pat. publication No.
20040163146)
The DNA constructs in TABLE 14 are constructed using the same methods as those described above, except that the PDK intron sequence (see Wesley et al., Plant J. 27:581-590 (2001)) was amplified using standard PCR techniques and operably linked to the remaining portions of the DNA construct (PDK Intron sequence and primers depicted in SEQ ID NO: 814-816).
TABLE 14
Final
Binary
Vector
Vector
Promoter
pARB554
pWVK147
Pinus radiata SuperUbiq + Intron (U.S. Pat.
No. 6,380,459)
pARB556
pWVK147
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
pARB557
pWVK147
Eucalyptus grandis COMT (U.S. Pat.
Publication No. 20040146904)
pARB558
pWVK147
Pinus radiate LIIM (U.S. Pat. publication No.
20040163146)
pARB514
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
No. 6,380,459)
pARB516
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
pARB518
pART29
Pinus radiata LIM (U.S. Pat. publication No.
20040163146)
The DNA constructs in TABLE 15 are constructed as described above and as follows. The YABBY intron sequence (see Foster et al., Plant Cell. 14(7):1497-1508 (2002)) is amplified using primers similarly designed to those above for the 4CL and PDK intron sequences and cloned into the vector backbone. Six additional fragments (fragments A through F and depicted in SEQ ID NOs: 789-795) are amplified with primers similarly designed to those used above. Primers for 4CL fragment A are designed to add a SmaI restriction sites to both ends of the amplified fragment; primers for 4CL fragment B are designed to add EcoRI and HindIII restriction sites at both ends of the amplified fragment; primers for 4CL fragment E are designed to add PstI restriction sites at both ends of the amplified fragment; and primers for 4CL fragment F are designed to add a SmaI restriction site to the one end and EcoRI and HindIII restriction sites to the other end of the amplified fragment. All seven fragments are cloned in the sense and antisense directions into the backbone vector as described above or by using the listed restriction enzymes. The complete RNAi cassette containing the promoter::sense fragment::intron::antisense fragment::3′UTR::nos terminator construct, is removed from the pBluescript plasmid as described above, and cloned into the binary vector pART27 or pART29 (digested with NotI). The binary vector pART29 is a modified pART27 vector (Gleave, Plant Mol. Biol. 20:1203-1207 (1992)) that contains the Arabidopsis thaliana ubiquitin 3 (UBQ3) promoter instead of the nos 5′ promoter and no lacZ sequences. Modifications to the promoter from the Pinus radiata Superubiquitin promoter plus intron to P. taeda 4CL, E. grandis COMT or P. radiata LIM promoters are as described above.
TABLE 15
Final
Binary
Vector
Vector
Promoter
Fragment
pARB318
pART27
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment A (SEQ
No. 6,380,459)
ID NO: 789)
pARB319
pART27
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment B (SEQ
No. 6,380,459)
ID NO: 790)
pARB320
pART27
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment C (SEQ
No. 6,380,459)
ID NO: 791)
pARB321
pART27
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment D (SEQ
No. 6,380,459)
ID NO: 792)
pARB322
pART27
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment E (SEQ
No. 6,380,459)
ID NO: 793)
pARB323
pART27
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment F (SEQ
No. 6,380,459)
ID NO: 794)
pARB324
pART27
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment G (SEQ
No. 6,380,459)
ID NO: 795)
pARB332
pART27
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment A (SEQ
ID NO: 789)
pARB333
pART27
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment B (SEQ
ID NO: 790)
pARB334
pART27
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment C (SEQ
ID NO: 791)
pARB335
pART27
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment D (SEQ
ID NO: 792)
pARB336
pART27
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment E (SEQ
ID NO: 793
pARB337
pART27
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment F (SEQ
ID NO: 794)
pARB338
pART27
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment G (SEQ
ID NO: 795)
pARB145
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment A (SEQ
No. 6,380,459)
ID NO: 789)
pARB146
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment B (SEQ
No. 6,380,459)
ID NO: 790)
pARB147
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment C (SEQ
No. 6,380,459)
ID NO: 791)
pARB148
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment D (SEQ
No. 6,380,459)
ID NO: 792)
pARB149
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment E (SEQ
No. 6,380,459)
ID NO: 793)
pARB150
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment F (SEQ
No. 6,380,459)
ID NO: 794)
pARB151
pART29
Pinus radiata SuperUbiq + Intron (U.S. Pat.
4CL fragment G (SEQ
No. 6,380,459)
ID NO: 795)
pARB183
pART29
Pinus taeda 4CL (2249 bp fragment of U.S.
4CL fragment A (SEQ
Pat. No. 6,252,135)
ID NO: 789)
pARB184
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment B (SEQ
ID NO: 790)
pARB185
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment C (SEQ
ID NO: 791)
pARB186
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment D (SEQ
ID NO: 792)
pARB187
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment E (SEQ
ID NO: 793)
pARB188
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment F (SEQ
ID NO: 794)
pARR189
pART29
Pinus taeda 4CL (U.S. Pat. No. 6,252,135)
4CL fragment G (SEQ
ID NO: 795)
The vector pARB310 (SEQ ID NO: 796) was developed by deleting several nonessential regions from the vector pBI121 (Clontech Laboratories, Palo Alto Calif.), replacing almost all of the DNA between the Right and Left Borders with a new multiple cloning site (Asc I, Not I, Apa I, Xho I, Sma I, Pst I, and Kpn I), and inserting a plant selectable marker comprising the UBIQUITIN3 (UBQ3) promoter from Arabidopsis (Norris, S. R. et al. (1993) Plant Mol. Biol. 21, 895-906) linked to the NPTII coding region and nos terminator. The barstar expression cassette from pMT416 (Hartley, R. W., J. Mol. Biol. 202:913-915 (1988)) was amplified using primers SEQ ID NO: 798 and 799 and cloned into an intermediate vector. The approximately 470 bp barstar fragment was obtained by digestion with BstX I and was subsequently clned into the BstX I site of pARB310 to yield the vector pARB310B.
The ColE1 replication origin and approximately 1 kb of flanking sequence was amplified from the vector pART27 (Gleave, Plant Mol. Biol. 20:1203-1207 (1992)) using the primers SEQ ID NO: 800 and 801. This ColE1 fragment was digested with BamH I and Bcl I, purified and ligated into the Bcl I site of pARB310B, between the end of the trfA gene and the left border (LB) of the T-DNA, to generate the vector pAGF50. pAGF50 was digested with Asc I and Nco Ito remove the UBQ3 promoter plus most of the NPTII coding region and the resulting 5.7 kb fragment was gel purified.
The 5′-end of the selectable marker cassette was replaced with a corresponding segment from plasmid pWVR3 (SEQ ID NO: 802), which had the promoter from UBIQUITIN10 (UBQ10) linked to the NPTII coding region. For the initial construction of the donor plasmid, the 1.3 kb promoter fragment of UBQ10, comprising ˜900 bp of upstream sequence, an untranslated exon of >40 bp, a ˜300 bp intron, and the initiation codon (Norris et al., Plant Mol. Biol. 21:895-906 (1993)), was amplified using PCR primers SEQ ID NO: 803 and 804. The NPTII coding sequence was amplified from pBI121 (Clontech laboratories, Palo Alto Calif.) using primers SEQ ID NO: 805 and 806, and the nopaline synthase transcription terminator (NOSTER) was amplified using primers SEQ ID NO: 807 and 808. The NPTII and NOSTER fragments were amplified separately in order to remove ˜300 bp of extraneous DNA found in pBI121. The primers UBQ10P3 and NPT2-5A are complementary to each other, which enabled the 3′-end of the promoter fragment to anneal to the 5′-end of the NPTII coding region fragment. A similar complementarity was used for the primers at the 3′-end of the NPTII fragment and the 5′-end of the terminator fragment, allowing the complete cassette to be formed without ligation. The three fragments were gel purified after being produced individually by PCR and were mixed with components of a normal PCR reaction (buffer, dNTPs, and TaqPlus Long polymerase). Each of the three fragments was present at approximately 10 ng/microL in a total of 20 microL. The mixture was denatured, then allowed to anneal and extend for 5 cycles. This reaction was then diluted to 200 microL with a fresh PCR reaction mixture, which included phosphorylated primers SEQ ID NO: 803 and SEQ ID NO: 808 for amplification of the full-length cassette, and underwent 10 further cycles. The resulting fragment was ligated into Sma I-digested pBluescript SK. After sequence verification, it was found that all isolated clones had mutations in them, thus non-mutated portions of two isolates were recombined to produce pWVR3. The 1.9 kb fragment with the UBQ10 promoter linked to the 5′-end of the NPTII coding region was released from pWVR3 by Asc I and Nco I digestion, gel purified, and ligated into the pAGF50 fragment to generate pARB1000.
Plasmid pARB1000 was modified by the addition of a SUBIN::GUSIN::nos terminator reporter cassette at the Sma I site to generate pARB1001 (SEQ ID NO: 809). (SUBIN is the Pinus radiata superubiquitin promoter plus 5′-UTR plus intron (U.S. Pat. No. 6,380,459), and GUSIN is the GUS coding region interrupted by the potato tuberin gene intron (Vancanneyt et al., Mol. Gen. Genet. 220:245-250 (1990)). The male-specific flowering control gene, PrMC2.400-1::barnaseH102E::RNS2TER, was present in pWVR219 (SEQ ID NO: 810), with an unwanted Not I site near the 3′-end. The plasmid was digested with Not I, and then the site was destroyed by treating with T4 DNA polymerase in the presence of dNTPs and religating the vector. The PrMC2.400-1::barnaseH102E::RNS2TER cassette was excised from the altered pWVR219 with Asc I and Xho I, and the 1.1 kb fragment was gel purified. pARB1001 was prepared by partial digestion with Xho Ito linearize the plasmid, followed by complete digestion with Asc I and purification of the 12.3 kb fragment. The PrMC2.400-1::barnaseH102E::RNS2TER cassette was ligated into the prepared pARB1001 vector to generate pARB1002 (SEQ ID NO: 811). The structure of the plasmid was verified with single-pass sequencing.
The (AtAGenh) PrAG::barnaseE73G::NOSTER cassette was removed from pWVCZ24 (SEQ ID NO: 812) by EcoR I and Asc I digestion. A Not I adapter comprising the oligonucleotides, EcoNot1 (5′-AATGCGGCCGCAGAGA-3′) and EcoNot2 (5′-TCTCTGCGGCCGC-3′), was ligated to the EcoR I site and digested with Not I, and then the 4.9 kb fragment was purified. The plasmid pARB1001 was digested with Not I and Asc I and the 7.6 kb vector fragment was gel purified. The above cassette was ligated into these sites to generate pARB1005L (SEQ ID NO: 813). The structure of the plasmid was verified with single-pass sequencing.
Example 15 demonstrates the assembly of a DNA contruct for use in expressing the monolignol synthesis CCoAOMT (Caffeoyl-coenzyme A o-Methyltransferase) gene in Pinus.
The vectors in TABLE 16 are cloned as described in Example 14 with the following changes. A fragment from the Pinus CCoAOMT gene (nucleotides 793-1016 of SEQ ID NO: 80 is amplified using standard PCR techniques. To clone the fragment in the sense orientation, the amplified fragment is cut with the restriction enzyme PstI, and cloned into the backbone vector. To clone the fragment in the antisense orientation, the amplified fragment is digested with ClaI and cloned into the backbone vector. The final DNA constructs are also modified by means of the addition of the PDK intron, the use of either the P. radiata Superubiquitin promoter with intron or the P. taeda 4CL promoter and the use of the pWVK147 binary vector using the methods described in Example 14.
TABLE 16
Final
Vector
Promoter
Fragment
pARB559
Pinus radiata SuperUbiq + Intron
Nucleotides 793-
(U.S. Pat. No. 6,380,459)
1016 of SEQ ID NO: 80
pARB560
Pinus taeda 4CL (U.S. Pat. No.
Nucleotides 793-
6,252,135)
1016 of SEQ ID NO: 80
Example 16 demonstrates the assembly of E. grandis CCoAOMT (Caffeoyl-coenzyme A O-Methyltransferase) DNA constructs.
The DNA constructs in TABLE 17 are cloned as described in Example 14, with the following modifications. A fragment from the E. grandis CCoAOMT (nucleotides 745-904 of SEQ ID NO: 223) is amplified using standard PCR tecnique in accordance with Example 15. The final vectors are also modified by the addition of the PDK intron or the Eucalyptus xylem intron which are well know in the art such as described by Wesley et al. 2001 Plant J. 27: 581-590, the E. grandis COMT promoter and the use of the pART29 binary vector using the methods described above.
TABLE 17
Final
Vector
Promoter::Intron
Fragment
pARB523
E. grandis COMT promoter::PDK
Nucleotides 745-
intron
904 of SEQ ID NO: 223
pARB524
E. grandis COMT promoter::
Nucleotides 745-
Eucalyptus xylem intron
904 of SEQ ID NO: 223
(International patent publication
no. WO00/22092)
Example 17 demonstrates the assembly of E. grandis CCR (cinnamoyl CoA reductase) DNA constructs.
The DNA constructs of TABLE 18 are cloned as described in Example 14, except that a fragment from the E. grandis CCR clone (nucleotides 1038-1326 of SEQ ID NO: 121) is amplified. The final vectors are also modified by the addition of the PDK intron or the Eucalyptus xylem intron which are well know in the art such as described by Wesley et al. 2001 Plant J. 27: 581-590, the E. grandis COMT promoter and the use of the pART29 binary vector.
TABLE 18
Final
Vector
Promoter::Intron
Fragment
pARB525
E. grandis COMT promoter::PDK
Nucleotides 1038-
intron
1326 of SEQ ID NO: 121
pARB526
E. grandis COMT promoter::
Nucleotides 1038-
Eucalyptus xylem intron
1326 of SEQ ID NO: 121
(International patent publication
no. WO00/22092)
Example 18 demonstrates the assembly of E. grandis C3H and C4H DNA constructs.
The DNA constructs in TABLE 19 cloned as described in Example 14, with the modifications that the fragments from the E. grandis C3H clones (SEQ ID NO: 817) or E. grandis C4H clones (SEQ ID NO: 191) is amplified using standard PCR tecnique in accordance with Example 15. Either the Arabinogalactan promoter (SEQ ID NO: 764) from E. grandis or the 4CL promoter of P. taeda (U.S. Pat. No. 6,252,135 as depicted therein as SEQ ID NO: 11) are operably linked to the C3H or C4H fragments. The P. radiata superubiquitin promoter intron vector is digested with the BamHI restriction enzyme using standard techniques. This fragment is cloned into a Bluescript vector containing either the 4CL promoter from P. taeda (digested with BamHI) or the Arabinogalactan promoter from E. grandis (digested with Clap. The P. taeda 4CL promoter and the E. grandis Arabinogalactan promoter are both amplified using primers similarly designed to those used to amplify the P. radiata superubiquitin promoter sequence with intron and then ligated into the base bluescript vector as described in Example 14. The final vector can also modified by the addition of the Pr4CL intron, and the use of the pARB1002 binary vector, using the methods described in Example 15.
TABLE 19
Final
Vector
Promoter
Fragment
pARB669
Eucalyptus grandis Arabinogalactan
SEQ ID NO: 817
promoter
(SEQ ID NO: 764)
pARB670
Eucalyptus grandis Arabinogalactan
SEQ ID NO: 191
promoter
(SEQ ID NO: 764)
pARB672
Pinus taeda 4CL promoter (2249 bp
SEQ ID NO: 191
fragment of U.S. Pat. application
6,252,135)
Example 19 demonstrates the assembly of DNA constructs for the modulation of lignin composition by increasing the percentage of sinapyl lignin monomers.
In this Example, the backbone vector pWVR5 was a pBI121 vector (Clontech laboratories, Palo Alto Calif.) with the 35S promoter GUS sequence removed and the NOS promoter replaced with the UBQ10 promoter from Arabidopsis (Sun, C. W. and J. Callis, Plant J., 11:101-111 (1997)).
The vector pARB459 was developed using the following steps. The Bluescript vector (Stratagene, La Jolla, Calif.) was modified by operably linking the Superubiquitin 3′UTR and nos 3′ terminator sequence to the Bluescript vector sequences. The resulting DNA construct was named pARB005 (SEQ ID NO: 775).
The P. radiata superubiquitin promoter with intron was added to pARB005. The promoter/intron sequence was first amplified from the P. radiata superubiquitin sequence identifed in U.S. Pat. No. 6,380,459 using standard PCR techniques and the primers depicted in SEQ ID NOs: 776 and 777. The amplified fragment was ligated into pARB005 to assemble the DNA construct pARB119 (SEQ ID NO: 778). The sweetgum (Liquidambar styraciflua) Cald5H gene (Osakabe et al., Proc Natl Acad Sci U.S.A. 96(16):8955-8960 (1999)) was then amplified using standard PCR techniques and the primers depicted in SEQ ID NOs: 779 and 780. The amplified fragment was ligated to pARB119 to produce the vector pARB459 (SEQ ID NO: 781).
The sweetgum Cald5H gene Cald5H gene (Osakabe et al., Proc Natl Acad Sci U.S.A. 96(16):8955-8960 (1999)) was cloned into pWVR5 to produce the DNA construct pWVC50 (SEQ ID NO: 757). pWVR5 was digested using NotI, separated on a 1% agarose gel, and purified. The purified DNA is treated with SAP (shrimp alkaline phosphatase) before the P. radiata superubiquitin promoter::Cald5H cassette is added and ligated using T4 DNA ligase. The P. radiata superubiquitin promoter::Cald5H terminator cassette was isolated from the vector pARB459 after digestion with NotI.
The E. grandis EGBA SAD gene (SEQ ID NO: 149) operably linked to the Eucalyptus Arabinogalactan promoter was cloned into the pWVR5 vector to produce the DNA construct pWVC51 (SEQ ID NO: 758). The vector pWVR5 was digested using NotI, separated on a 1% agarose gel, and purified. The purified DNA was treated with SAP (shrimp alkaline phosphatase) before the EGBA SAD gene was added and ligated using T4 DNA ligase. The Euc Arabinoglactan promoter::EGBA SAD::ter cassette was isolated from the vector pARB487 after digestion with NotI.
The vector pARB487 can be derived using the following steps. The Arbinogalactan promoter was isolated as described above and operably linked to the E. grandis EGBA SAD gene (SEQ ID NO: 149) using PCR primers having unique cloning sequences. This fragment was used to assemble the DNA construct pARB453. The Euc Arabinoglactan promoter::EGBA SAD::ter cassette was removed from pARB453 by digesting the DNA with NotI and ligated into the NotI site of pART29 to assemble the DNA construct pARB487.
The sweetgum BioMT gene can be cloned into the pWVR5 vector to produce the vector pWVC55 (SEQ ID NO: 759). The vector pWVR5 was digested using NotI, separated on a 1% agarose gel, and purified. The DNA was treated with SAP (shrimp alkaline phosphatase) before the BioMT gene fragment was added and ligated using T4 DNA ligase. The P. taeda 4CL promoter::sweetgum BioMT::3′UTR/nos terminator fragment was isolated from the vector pARB257 after digestion with NotI.
The vector pARB257 was assembled as follows. The P. taeda 4CL promoter of U.S. Pat. No. 6,252,135 is amplified using PCR. The sweetgum BioMT gene was amplified using PCR primers (SEQ ID NOs: 782 and 783) having unique restriction ezyme sequences. The fragment was then used to assemble the DNA construct pARB156. The P. taeda 4CL promoter::sweetgum BioMT::3′UTR/nos terminator casesette was removed from pARB156 by digesting the vector with NotI and ligated into the NotI site of pARB5 to assemble the DNA construct pARB257.
In order to assemble the DNA construct pWVC56 (SEQ ID NO: 760), the DNA construct pWVC52 was assembled first. The Eucalyptus Arabinogalactan promoter::EGBA SAD fragment was removed from pWVC51 (SEQ ID NO: 758) using the restriction enzyme KpnI. This fragment and the P. radiata superubiquitin promoter::Cald5H gene from pARB459 (as described above) were cloned into the pWVR5 vector sat the NotI site. This construct was analyzed using standard techniques for the presence of both inserts in the required orientation. The resulting construct was named pWVC52.
pWVC56 (SEQ ID NO: 760) was constructed by removing the P. taeda 4CL promoter from pWVC55 (SEQ ID NO: 759) using the restriction enzymes EcoRV and SbfI. The resulting fragment was ligated with pWVC52 after that DNA construct was digested with the restriction enzymes SrfI and SbfI. The final plasmid was verified by restriction digest using standard methods.
The control DNA construct pWVR31 was engineered from pWVR8 (Arabidopsis ActinII::GUSINT, UBQ10::NPTII). The UBQ11 promoter from Arabidopsis (Norris et al., Plant Mol Biol. 21(5):895-906 (1993)) was amplified by PCR using the primers SEQ ID NO: 771 and 772. This fragment was then cloned into pWVR8 in place of the ActinII promoter. The resulting construct was pWVR31.
Example 20 demonstrates the assembly of DNA constructs for use in Arabidopsis complementation experiments.
The DNA construct pARB460 (SEQ ID NO: 762) was constructed by removing the P. radiata superubiquitin promoter::Cald5H cassette from pARB459 (described above in Example 19) using the restriction enzyme NotI. The resulting fragment was cloned into the NotI site of pART27 (Gleave et al., Plant Mol. Biol. 20:1203-1207 (1992)).
The DNA construct pARB373 (SEQ ID NO: 763) was constructed as follows. The E. grandis Arabinogalactan promoter was initially isolated as described in Example 19. This fragment was then cloned into pARB005 (described above in Example 19) to assemble pARB154. The sweetgum Cald5H gene (Osakabe et al., Proc. Natl. Acad. Sc.i U.S.A. 96(16):8955-60 (1999)) was then cloned into pARB154 in the sense orientation operably linked to the Arabinogalactan promoter. The resulting construct was pARB262 (SEQ ID NO: 786). The E. grandis Arabinogalactan promoter::Cald5H:: 3′UTR/nos terminator cassette was removed from pARB262 using NotI and cloned into the NotI of pART27 (Gleave et al., Plant Mol. Biol. 20:1203-1207 (1992)) to assemble pARB373.
The DNA construct pARB595 (SEQ ID NO: 784) was assembled as follows. The Eucalyptus Cald5H gene (SEQ ID NO: 186) was amplified using standard PCR techniques. The amplified fragment was then ligated into pARB119 to assemble pARB594. The SuperUbiquitin promoter::EucCald5H::3′UTR/nos terminator cassette was removed from pARB594 and cloned into the NotI of pART27 (Gleave et al., Plant Mol. Biol. 20:1203-1207 (1992)) using standard techniques to produce pARB595.
The DNA construct pARB597 (SEQ ID NO: 785) was assembled as follows. The Eucalyptus Cald5H gene (SEQ ID NO: 185) was amplified using standard PCR techniques. The amplified fragment is then ligated into pARB119 to assemble pARB596. The SuperUbiquitin promoter::EucCald5H::3′UTR/nos terminator cassette was removed from pARB596 and cloned into the NotI of pART27 (Gleave et al., Plant Mol. Biol. 20:1203-1207 (1992)) using standard techniques to produce pARB597.
Example 21 demonstrates the transformation of Arabidopsis plants with the inventive DNA constructs of Example 20.
Arabidopsis fah1 mutant plants were transformed with Agrobacterium containing the DNA constructs of Example 20 by floral dip infiltration. Briefly, Agrobacterium cultures were centrifuged at ˜8600 rcf for 10 minutes at 20° C. and were resuspended to an optical density of ˜0.7-0.8. Plants were dipped into an infiltration solution containing the Agrobacterium for about 5 seconds. Plants were drained of excess solution and placed under grow lights in ambient conditions. After about 24 hours, the plants were misted and maintained for seed production. T1 seeds were surface sterilized in 5% commercial bleach solution and plated on MS media containing Kanamycin (50 mg/l) and Timentin (250 mg/l) to select for putative transformants.
Once selected, putative transformants were transferred to rockwool and grown for four weeks before testing.
Example 21 demonstrates the modulation of lignin composition in Arabidopsis plants transformed with the inventive DNA constructs of Example 20.
The Arabidopsis fah1 mutant was defective in ferulate 5-hydroxylase. See Chapple et al., Plant Cell. 4(11):1413-1424 (1992). In this mutant Arabidopsis plant, lignin composition was marked by the complete absence of syringyl (S) subunits (Marita et al., Proc. Natl. Acad. Sci. U.S.A. 96(22):12328-12332 (1999)). Likewise, the mutant plant was completely devoid of sinapoyl esters. The inventive DNA constructs of Example 20, pARB595 and pARB597, were transformed into Arabidopsis fah1 mutant plants using the transformation method described in Example 21.
HPLC analysis (Agilent HPLC 1100 series—Germany) was used to determine the presence of sinapoyl malate in the transformed plants, fah1 mutant plants, and wild-type Arabidopsis plants. HPLC was performed using standard procedures. In brief, leaf extracts were analysed by both UV and mass spectrometry (Agilent Mass Spec 1100 series LC/MSD Trap—Germany) in each run. The instrument diode array detector was set to measure UV absorbance at 330 nm. The Ion Trap mass spectrometer was operated in negative mode ionisation to detect chemical species that could be deprotonated, e.g., those chemical species containing acidic groups such as sinapoyl malate. During the gradient, a spectrometric peak was observed on the UV 330 nm trace corresponding to a peak giving rise to a spectrum whose major components were singly charged and had mass to charge (m/z) ratios of 339.2 and 223.1. Sinapoyl malate (C15H16O9) has a molecular weight of 340.28 g/mol—once deprotonated a skilled artisan would expect to see a peak with a mass to charge ratio of 339.28. The m/z 339.2 species was isolated in the ion trap and when fragmented can be found to give rise to the m/z 223 species. The 223 m/z ratio equates to a species that one skilled in the art would expect from the deprotonated sinapoyl moiety from sinapoyl malate. The m/z 223 species can be isolated in the ion trap and if fragmented can give gave rise to a spectrum that a skilled artisan would understand accounts for the structure of the sinapoyl moiety.
Accordingly, those skilled in the art would know that the peak of interest in the chromatogram is sinapoyl malate that has been fragmented into the sinapoyl species before reaching the trap due to in-source collision induced dissociation (CID). This can be confirmed by varying the skimmer voltage to reduce (CID). If done, this action can allow tha capture of more intact sinapoyl malate.
As can been seen in
Example 23 demonstrates the staining of a sample from the transformed Arabidopsis fah1 mutant plants of Example 22.
Hand-cut stem and hypocotyls samples from a pARB595-transformed Arabidopsis fah1 mutant plant of Example 22, an Arabidopsis fah1 mutant plant, and a wild-type Arabidopsis plant were stained with Maule reagent. Proctols for staining plant tissue with Maule reagents are well known in the art, and a detailed descrition can be found at Strivastava L M, T.A.P.P.I. 49:173-183 (1966). In short, Maule reagent allows the determination of the level of syringyl ligin in a plant sample. Samples were scored for the presence or absence of stain on a semi-quantitative scale (− to +++). TABLE 20 presents the staining results for a pARB595-transformed Arabidopsis fah1 mutant plant of Example 22, an Arabidopsis fah1 mutant plant, and a wild-type Arabidopsis plant.
TABLE 20
pARB595-
Transformed
Arabidopsis fah1
Arabidopsis fah1
Wild-Type
Mutant Plant
Mutant Plant
Arabidopsis Plant
Stem
+++
+
−
section
Hypocotyl
+++
+
−
section
As indicated in TABLE 20, the transformation of a Arabidopsis fah1 mutant plant correlates with the increased production of syringyl lignin, even in excess of the syringyl lignin present in wild-type Arabidopsis plants. Accordingly, those skilled in the art would recognize the increase in sinapoyl malate observed in Example 22 correlates to an increase in syringyl lignin in transformed Arabidopsis fah1 mutant plants.
Example 24 demonstrates the transformation of Eucalyptus grandis with the DNA constructs of Example 20 and the growth and propagation of transgenic E. grandis plants.
pARB373 (SEQ ID NO: 763) and pARB460 (SEQ ID NO: 762), as described in Example 20, were used to transform clonal E. grandis leaf explants. The leaf explants were transformed according to the protocol described in International patent publication WO00/12715, except where noted below. In brief, dissected leaf explants were inoculated with Agrobacterium comprising the DNA constructs pARB373 or pARB460. Inoculated explants were co-cultured for two weeks in diffuse light and selected on agar supplemented with 250 mg/L kanamycin and 250 mg/L timentin (omitting NAA from the transformation media). Leaf explants were then cultured for two weeks on on agar supplemented with 100 mg/L kanamycin and 250 mg/L timentin. The leaf explants were cultured for another two weeks on on agar supplemented with 150 mg/L kanamycin and 250 mg/L timentin. Thereafter and until healthy single shoots were collected, the leaf explants were transferred monthly to fresh media containing 150 mg/L kanamycin and 250 mg/L timentin.
Single shoots were place in elongation media in order to proliferate the putative transgenic tissue. The alongation media consists of Murashige and Skoog salts (MS) supplemented with 1 microM 6-benzylaminopurine (BAP), 20 g/L sucrose and 7 g/L agar. PCR analysis of the explant tissue was conducted after approximately 200 mg of tissue is grown and collected. Both the promoter and gene sequences were verified using PuRe Taq Ready-To-Go™ PCR beads (Amersham Biosciences, Piscataway, N.J.). PCR positive explants were then then maintained as sock cultures through proliferation on elongation media supplemented with 150 mg/L kanamycin and 250 mg/L timentin.
Transgenic E. grandis plants were propagated from these stock cultures. Where necessary, shoots were transferred monthly to fresh media. Single shoots were placed onto elongation media and maintained until reaching approximately 2-3 cm tall. Thereafter, single shots were placed into conventional rooting medium. After 10 days, the transformed plants are transferred to a green house with appropriate climate. A skilled artisan would recognize that many different culture media and intervals may be suited to regenerating plants of the instant invention. Using an appropriate humidity regime and fungicides to control fungal growth, transgenic plants were grown in the greenhouse for 6 months in potting mixture. In doing so, the transgenic plants were grown in a meshed compartment at ambient temperature with capillary watering. Plants were potted into 5 L poly-bags in s soil-less peat based compost supplemented with a slow release fertilizer.
A field test of pARB460-transformed E. grandis plants was established in Florida, USA in November 2003. This test comprised of about 20 different lines of pARB460-transformed E. grandis plants of about 8 ramets each.
Likewise, pARB373-transformed E. grandis plants were tested in Florida, USA in November 2003. This field test comprised of about 20 different lines of pARB373-transformed E. grandis plants of about 8 ramets each. A second planting of pARB373-transformed E. grandis plants was established in Florida, USA in May 2004. This test comprised of about 6 different lines of 2 ramets each. The same six translines and 4 ramets of each were also established in a field test in South Carolina, USA in May 2004.
Example 25 demonstrates the testing of lignin content and other phenotypic traits in the transformed E. grandis plants of Example 24.
The transformed E. grandis plants of Example 24 were sampled at approximately 6 months of age. The bottom 20 cm of the stem was collected from each transformed plant. The bark, phloem and the primary cortex was removed from the stem by peeling. Stem samples were then flash frozen in liquid nitrogen, and freeze-dried in a Flexi-Dry Microprocessor Control—Corrosion Resistant Freeze-Drier (Stone Ridge, N.Y., USA) according to the manufacturer's instructions. Samples were ground in a Wiley Mill (Arthur H. Thomas Co,; Philadelphia, U.S.A) and then re-ground in a ring mill. Ground samples are then dried for a minimum of 1 day at 55° C. and stored at this temperature until used. Cell wall material was isolated from the samples in a series of stages by suspending the ground material in the solvent or solution, extracting with an ultrasonic cleaner, centrifuging and decanting off the supernatant. The following sequence of extractions was used: (1) NaCl at two concentrations; (2) aqueous ethanol; (3) CHCl3:MeOH; and (4) acetone. To remove starch, the extracted cell wall materials were washed, heated in tris-acetate buffer to gelatinize the starch and then treated with α-amylase. Following enzyme treatment the suspensions were centrifuged and the resulting precipitate washed with ethanol and acetone, allowed to stand overnight, and then dried at 55° C. The isolated cell materials were used for small scale lignin determinations using the procedure described in Fukushima, R. S. and R. D. Hatfield, J. Ag. Food Chem. 49(7):3133-9 (2001).
Results from the Fukushima and Hatfield determinations of lignin content are shown in
Likewise, the height of pARB373-, pARB460-, and control construct-transformed E. grandis plants were compared. All measurements were taken on whole plants before sampling. The average heights and lignin content, as reported above, of pARB373-, pARB460-, and control construct-transformed plants are shown in
Accordingly, even though lignin content is similar in each of the transformed plants, additional phenotypic changes, such as growth rate and average height, are effected by the modulation of monolignol synthesis genes.
Example 26 demonstrates the analysis of lignin composition in the transformed E. grandis plants of Example 24.
Cell wall materials from the transformed E. grandis plants of Example 24 were isolated and prepared according to the methods described in Example 26. Once prepared, cell wall materials were analyzed for lignin composition using the DFRC technique as described by Lu, F. and J. Ralph, J. Agric. Food Chem. 45(7):2590-2592 (1997). Breifly, DFRC selectively and efficiently cleaves alpha-ether and beta-ether linkages to allow for the quantitative analysis of lignin subunits. The lignin-containing sample was dissolved in an acetyl bromide stock solution by gentle stirring at 50° C. for about 2 hours. Then, the volatile solvent and reagent were removed by rotary evaporation at less than about 40° C. with the addition of acetone. The residue was then dissolved in dioxane/acetic acid/water (5/4/1 by volume) After being stirred well, 50 to 100 mg of Zn dust is added. The resulting mixture was stirred continuously for 30 minutes and then extracted into methyllene chloride to give a degradation product. These products were then acetylated with Ac2O/pyridine (1:1) for about 40 minutes.
As determined by DFRC, the lignin composition of the cell wall materials are shown in
As can be seen in
In addition,
Example 27 demonstrates the transformation and propagation of Pinus plants.
The inventive DNA constructs were used to transform a Pinus plant. Any method known to those skilled in the art can be used. For example, specified clones of elite selected families of loblolly pine (Pinus taeda), and a particular clone of hybrid pine (P. taeda×P. rigida) can be initiated as embryogenic cell lines from zygotic embryos of individual immature megagametophytes using the procedures described in U.S. Pat. No. 5,856,191, and maintained using the procedures described in U.S. Pat. No. 5,506,136.
After one to three months of culture on maintenance medium, the tissue cultures were cryopreserved, stored for periods of up to several years, and retrieved using the methods of U.S. Pat. No. 6,682,931. Those skilled in the art of plant tissue culture will recognize that other cryopreservation and recovery protocols would be applicable to the present method and that the detail in this example may not be construed to limit the application of the method.
Uniform suspension cultures from each of the genetically different tissue culture lines were established by inoculating a 250 ml Nephelo sidearm flask (Kontes Chemistry and Life Sciences Products) with 1 g of tissue each according to the method of U.S. Pat. No. 5,491,090. The flasks containing the cells in liquid medium are placed on a gyrotory shaker at 100 rpm in a dark culture room at a temperature of 23° C.±2° C. One week later, the liquid in each flask was brought to 35 ml by pouring 15 ml fresh medium into the culture flask and swirling to evenly distribute the cells. Cell growth was measured in the sidearm by decanting cells and medium into the sidearm portion of the flasks, allowing the cells to settle for 30 minutes and then measuring the settled cell volume (SCV). When the SCV was greater than or equal to half the maximal SCV (50% of the volume of the flask was occupied by plant cells), each culture was transferred to a 500 ml sidearm flask containing a total of 80 ml cells and medium and the transferred culture was maintained under the same conditions.
To prepare for gene transfer, polyester membrane supports are sterilized by autoclaving and placed in separate sterile Buchner funnels, and for each of six replicate plates per cell line, one to three milliliters of pine embryogenic suspension was pipetted onto each support such that the embryogenic tissue is evenly distributed. The liquid medium was suctioned from the tissues and each support bearing the embryogenic tissue is placed on gelled preparation medium for Agrobacterium inoculation according to the methods described in U.S. Patent Publication No. 20020100083. Specifically, the binary constructs of SEQ ID: 757-761 were each introduced into different isolates Agrobacterium tumefaciens by techniques well known to those skilled in the art, and virulence was induced with administration of acetosyringone by commonly used techniques whereupon each of the induced Agrobacterium isolates was co-mingled with separate replicates of the plant material according to the methods described in U.S. Patent Publication No. 20020100083. Additionally, certain replicates of the plant material were co-mingled with Agrobacterium containing a mixture of equal amounts of the binary constructs of SEQ ID: 757-759 for contransformation. The cells were co-cultivated in the dark at 22°±2° C. for approximately 72 hours.
Following co-cultivation, Agrobacterium was eradicated from the cultures according to the methods described in U.S. Patent Publication No. 20020100083. Cells borne on polyester membrane supports were then transferred onto fresh selection media at intervals of 2 weeks. Active growth on the selection medium occurred in a number of isolated sectors on many of the petri dishes. Such active growth in the presence of selection agent was normally an indication that the growing tissues have integrated the selection gene into their chromosomes and are stably transformed. These areas of active growth are treated as independent transformation events and are henceforth referred to as putative transgenic sublines. The putatively transgenic embryogenic tissue was multiplied by transferring growing transgenic sectors to fresh semi-solid maintenance medium supplemented with the respective selection agent.
Putatively transformed sublines, after reaching approximately 2 g, were chosen for polymerase chain reaction (PCR) amplification for verification of the presence of transgenes using standard techniques. Lines that had been verified by PCR as co-transformed with any one, two, or three of the three constructs of SEQ ID 757-759 were selected for testing alongside lines transformed with the control construct of SEQ ID: 761 and the three-gene construct of SEQ ID 760, in order to verify the hypothesis that any production of syringyl pathway intermediates could be attributed only to the presence of all three genes, and to allow discovery of new intermediates that might be produced by any one gene or two-gene combination in the inventive gymnosperm cells or plants.
Germinable embryos were produced from each of the selected lines verified as transformed by PCR, as follows. After the cell masses cultured on selection medium have proliferated to at least one gram, each culture was separately resuspended in liquid medium. When the cell suspensions were brought to uniform (half-maximal) SCV, equivalent amounts of suspension culture cells were pipetted onto sterile membrane supports for placement on development/maturation medium as described in U.S. Pat. No. 5,506,136 to develop high quality harvestable stage 3 (cotyledonary) embryos. Dishes were incubated in a dark growth chamber at 23±2° C. The membrane supports were transferred to new petri dishes containing fresh medium every 3 weeks. At week 9, stage 3 (cotyledonary) embryos were visually analyzed for germination quality and harvested onto fabric supports on medium as described in U.S. Pat. No. 5,506,136, and incubated for about four weeks in the dark at a temperature of 4° C.±2° C. Next, embryos on their fabric supports were incubated above water in sealed containers for about three weeks in the dark at a temperature of 25° C.±2° C. Following the above two treatments, embryos on their fabric supports were transferred to medium germination medium and incubated for about three days in the dark at a temperature of 25° C.±2° C. Embryos were then removed from their fabric supports and placed onto the surface of fresh germination medium. Germination was conducted in the light at a temperature of 25° C.±2° C. Germination plates were examined weekly, over a period of about four weeks, and germinating embryos were transferred to MAGENTA® boxes containing 100 ml of germination medium for conversion to plantlets. MAGENTA® boxes containing developing plantlets were incubated in the light at 25° C.±2° C. for about eight to twelve weeks.
When the plantlets form epicotyls (newly formed shoots of approximately two to four cm), they were transferred to containers filled with a potting mix [2:1:2 peat:perlite:vermiculite, containing 602 g/m3 OSMOCOTE fertilizer (18-6-12), 340 g/m3 dolomitic lime and 78 g/m3 MICRO-MAX micronutrient mixture (Sierra Chemical Co.)]. The plantlets were grown in a shaded greenhouse and misted infrequently for a period of about two weeks. They were removed from mist for acclimatization in the greenhouse for about four weeks. Plantlets were then transferred to outdoor shade for about six weeks for final acclimatization before moving to full-sun conditions. They were then grown in containers until conditions were ready for field planting.
Once transformed and propagated, a skilled artisan would also recognize the accelerated reproduction of Pinus plants can occur by grafting of the plantlets. See, e.g., Mergen, F. (1954) Rooting and grafting of slash pine (Pinus elliottii Engel.) for application in forest genetics. Ph.D. dissertation, Yale University, New Haven, Conn.; and Ahlgren, C. E. (1967) A relationship between scion, bud origin and growth of white pine grafts. Minnesota Forestry Notes 180. University of Minnesota, St. Paul. 2 p.
Example 28 demonstrates histologic staining of the tramsformed P. taeda plants of Example 27.
Samples were taken from 8 month-old P. taeda plants were transformed and propagated as described in Example 27. One plant was transformed with a DNA construct comprising SEQ ID NO: 760. Another plant co-transformed with DNA construct comprising SEQ ID NOs: 757-759. Another plant co-transformed with DNA construct comprising SEQ ID NOs: 757 and 759. In addition, control P. taeda trees or Populus deltoides (cottonwood) trees about 6 months old were sampled. Samples were taken from the lower stem of the plants, and sectioned with a Uchida sliding sledge microtome (EM Scientific) to obtain sections approximately 40 μm thick. Sections were then stained with toluidine blue, phloroglucinol (1,3,5-trideoxybenzene; FW=126.1), and Maule and stains.
Toluidine blue is a general cellular stain used to assist in the delineation of cell types such as parenchyma, xylem and phloem in the cross sections. Phloroglucinol, also known as the Weisner reagent, is a stain for lignin (Pomar et al., Protoplasma. 220(1-2):17-28 (2002)), and Maule stain is used to detect specifically syringyl lignin subunits (Lewis et al., Annu. Rev. Plant Physiol. Plant Mol. Biol. 41: 455-496 (1990)).
To stain sections with toluidine blue, sections were placed in 50 mM Tris-HCL pH 8.0 as soon as they were cut until all the sections were collected. The Tris buffer was replaced with enough 0.05% aqueous toluidine blue and left for 1 minute. The sections were then rinsed with water before images were captured with a Spot RT Color Camera under a Wild Heerburgg dissecting microscope.
To stain sections with phloroglucinol, sections were placed in 50 mM Tris-HCL pH 8.0 as soon as they were cut until all the sections were collected. The Tris buffer was then replaced with 1% (w/v) phologlucinol and the sections stained for 15 minutes before images were captured with a Spot RT Color Camera (Diagnostics Instruments) under a Wild Heerburgg dissecting microscope (Iiyama et al., Wood Sci. Technol. 22:167-175 (1988)).
To stain sections with Maule, sections were placed in 50 mM Tris-HCL pH 8.0 as soon as they were cut until all the sections were collected. The Tris buffer was replaced with enough 1% (w/v) KMnO4 to completely wet all the sections and incubated at room temperature for 5 minutes. The sections were rinsed with 10 volumes of water and then covered with enough 3% (v/v) HCl to wet the sections. This was left at room temperature for 10 minutes and then replaced with enough NH4OH to completely wet the tissue. After a minimum of 2 minutes the sections were mounted in water and images were captured immediately with a Spot RT Color Camera under a Wild Heerburgg dissecting microscope and rated on a scale of 1 to 5 for brightness of stain (Speer E. O., Stain Technol. 62(4):279-280 (1987)).
Staining of each blind-labeled sample was rated for intensity by three independent observers. The results are compiled in
Accordingly, the samples were further examined. Next, stem sections were either directly stained with phloroglucinol or Maule as described above or pre-treated for extensive extraction of soluble compounds before staining. Pre-treatment involved placing stem sections in a microfuge tube with 80% ethanol, floating the tubes in a Branson 1510 sonicator and sonicating the samples for 30 minutes with ethanol changes every 10 minutes.
One positive staining sample from each set of trees transformed with either SEQ ID NO: 760 or co-transformed with SEQ ID NOs: 757, 758 and 759, a negative staining sample transformed with SEQ ID NO: 761 and an untransformed Eucalyptus grandis seedling stem section, which should show the heavy Maule staining typical of an angiosperm (use in this experiment because the age of the wood was comparable to that of the pine transformants, while the cottonwood control that had been used in the initial exploratory experiment described above was older) were stained both with and without an ethanol-sonication extraction pretreatment. The sections were rated on a semi-quantitative scale of − to +++ for intensity of staining and the results are listed in TABLE 21.
TABLE 21
Maule +
Phloroglucin +
SEQ ID
Maule
pretreatment
Phloroglucinol
pretreatment
760
+++
+++
+++
+++
757,
+
+
+++
+++
758 &
759
761
−
−
+++
+++
E. grandis
+++
+++
+++
+++
If the compounds stained in the previous experiment using Maule or phloroglucinol were in fact soluble lignins in the cytosol a skilled artisan would have expected a substantial difference in staining intensity between the samples that were pre-treated and those that were not pre-treated. Since no difference was observed between pre-extracting the wood of pine samples and not pre-extracting the wood of pine samples in which all three genes were added by transformation, those skilled in the art would assume that the compounds produced in the stained three-gene transformant plants are not soluble and thus likely to be incorporated into the cell wall. The staining observed in this example is consistent with that observed in the pyrolysis molecular beam mass spectrometry results of Example 29 with plants co-transformed with SEQ ID NOs: 757, 758 and 759 not producing as much syringyl lignin as those transformed with SEQ ID NO: 760. Both these examples strongly support the claim that the enzyme produced by the gene of SEQ ID NO: 758 has a sinapylaldehyde dehydrogenase function which, in combination with a Cald5H enzyme and an OMT enzyme added by transformation to a gymnosperm, can produce syringyl lignin monomers that are incorporated into the wood cell walls.
Example 29 demonstrates the analysis of plant lignin composition by pyrolysis molecular beam mass spectrometry.
Loblolly pine trees were' transformation and propagation as described in Example 27. Samples were collected from the same transformed plants as described in Example 28 at 4 months. In addition, samples were obtained from a loblolly pine untransformed control and a mature aspen untransformed control. All samples were obtained by cutting approximately 20 mg of tissue from each stem. Each sample was weighed in a quartz boat, and pyrolyzed in a reactor consisting of a quartz tube (2.5 cm inside diameter) with helium flowing through at 5 L/min (at STP). The reactor tube was placed such that the sampling orifice of the molecular-beam mass spectrometer was inside the end of the quartz reactor. A custom-built molecular-beam mass spectrometer using a Extrel™ Model TQMS C50 mass spectrometer was used for pyrolysis vapor analysis as described in R. J. Evans and T. A. Milne, Energy & Fuels 1:123-37 (1987), and J. C. del Rio et. al., (2001) J. Anal. Appl. Pyrolysis 58-59:425-439 (2001). The reactor was electrically heated and its temperature maintained at 550° C. Total pyrolysis time was 90 seconds although the pyrolysis reaction was completed in less than 50 seconds. The residence time of the pyrolysis vapors in the reactor pyrolysis zone has been estimated to be ˜75 ms and is short enough that secondary cracking reactions in the quartz reactor are minimal. Mass spectral data from 20-450 Da were acquired on a Teknivent Vector 2™ data acquisition system using 22 eV electron impact ionization. Using this system, both light gases and heavy tars are sampled simultaneously and in real time. The mass spectrum of the pyrolysis vapor provides a rapid, semiquantitative depiction of the molecular fragments.
Duplicate mass spectra of the loblolly pine sample set and standards were collected on 2 successive days in a block fashion so as to mitigate problems associated with data analysis that could arise from day to day spectrometer drift. A combined analysis of the mass spectra collected on both days indicated that minimal spectrometer drift occurred.
Spectra from each of the samples were examined. Particular attention was given to the peaks arising from the pyrolysis of lignin break-down products. The assignment of mass spectra peaks associated with pyrolysis molecular beam mass spectroscopy of loblolly pine wood samples was described in Evans & Milne (1987) and those assigned to lignin break-down products and monomers are listed in TABLE 22.
TABLE 22
m/z
Assignment
124
guaiacol3
150
vinylguaiacol3
154
syrignol2
164
propenyl guaiacol2
168
4-methyl-2,6-dimethoxyphenol2
194
4-prophenylsyringol2
210
Sinapylalcohol2
2851
Dehydroabietic acid3
302
abietic acid3
NOTES: 1fragment ion, 2syringyl monomer, 3guaiacyl monomer
As can be seen in
TABLE 23
SEQ ID
propenyl
4-methyl-2,6-
dehydroabietic
abietic
NO
Guaicol
vinylguaicol
guaicol
syringol
dimetoxyphenol
4-propehylsyringol
sinapylalcohol
acid
acid
760
−7.45
−1.95
−0.32
95.54
57.14
47.69
99.00
12.49
12.94
757, 758
1.92
0.02
6.03
73.96
3.10
44.27
45.22
−5.62
−13.90
and 759
A skilled artisan would conclude that increases in some of the syringyl breakdown products are observed in plants transformed with SEQ ID NO: 760 or co-transformed with Seq ID NOs: 757-759. The observed increases in syringyl breakdown products were greater when the genes used in SEQ ID NOs: 757-759 are not co-transformed into a tree but transformed as a single vector as in SEQ ID NO: 760. These measured increases in syringyl lignin breakdown products in plants transformed with syringyl lignin vectors suggest that more syringyl lignin was formed in transformed plants than in controls, but these measurements do not reveal if the increased syringyl lignin had been incorporated into the cell wall.
Example 30 demonstrates use of transformed Pinus plants to increase pulping efficiency in the commercial wood pulping and papermaking industry.
Wood possessing increased percentages of syringyl subunits has been shown to have increased pulping efficiency. See Huntley et al., J. Agric. Food Chem. 51(21):6178-6183 (2003). Pinus plants transformed with the inventive DNA, and more particularly SEQ ID NOs: 185-186 or 762-763, can also produce wood with increased pulping efficiency.
To determine whether reduced lignin content or altered lignin composition correlates to improvements in the pulping process, the inventive transformed plants are subjected to micro-pulping. Micro-pulping can be used to assess parameters for the determination of the suitability of wood for Kraft pulping. These parameters are pulp yield, pulping rate, alkali consumption, fibre qualities and pulp bleachability. For the inventive plants, these parameters are tested as follows.
Wood samples are air dried, chipped and then oven dried at 105° C. for at least two days and until a constant weight is reached. Kraft pulping is performed in 150 mL stainless steel reactors attached to the rotating arm of a Stalsvets multi-digester pulping unit (Stålsvets, Sweden). The reactors are rotated through a polyethylene bath heated by electric heaters having a total capacity of 12.5 kW and controlled by an Omron controller (Omron Corporation, Illinois, USA) Typical pulping conditions are:
Effective alkali charge: 14% (as Na2O)
Liquor sulphidity: 30%
Liquor:wood ratio: 6:1
Maximum pulping temperature: 170° C.
Time to maximum temperature: 90 minutes
H-factor: Determined by varying the time at 170° C.
Those skilled in the art of pulp manufacture will recognize that many other combinations of micropulping conditions are available to test the pulpability of the inventive wood. Subsequently, the reactors are quenched in cold water, and the cooked chips filtered off on a Buchner funnel. The filtrate is retained for residual alkali analysis. The cooked chips are washed extensively with tap water and then blended for 15 minutes in a standard British disintegrator. The resulting pulp is filtered on a Buchner funnel and washed with water until the filtrate is clear. The pulp pad is dried overnight at 60° C., and total yield determined by weighing.
Residual alkali is determined by titration with 0.5 M hydrochloric acid to the first inflection point. See Milanova et al., Nordic Pulp and Paper Research Jl. 9(1):4-9 (1994). Alkali consumption is generally understood to be the difference between the effective alkali charge on chips and residual alkali in the black liquor, expressed as a percentage of oven-dry chips (as Na2O).
Pulp kappa number is determined by a half scale modification of Appita Standard 201m-86 (AS/NZS 1301.201s:2002). The pulping rate is calculated as the kappa number reached for a given cooking time.
Pulp bleachability is determined by bleaching pulps at 10% consistency using a D-Eo-D sequence (see Kibblewhite et al., Appita 51(2):1145-1121 (1998)) as follows:
Following bleaching, 5 g brightness pads are prepared at about pH 4.0 to 5.5, and brightness is determined after equilibration at 23° C. and 50% RH using a L & W Elrepho (Lorentzen & Wettre, Kista, Sweden). Fiber qualities such as average fiber length, width, and lumen size and standard deviations are analysed using a Kajaani FibreLab system (Metso Automation, Kajaani, Finland).
The results are correlated to the type of construct used in the transformation and demonstrate that the constructs effectively modulate the suitability of the wood resources for Kraft pulping
While the invention is described with reference to exemplary embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this invention. All references and publications cited herein are incorporated by reference in their entireties.
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The patent contains a lengthy table section. A copy of the table is available in electronic form from the USPTO web site (). An electronic copy of the table will also be available from the USPTO upon request and payment of the fee set forth in 37 CFR 1.19(b)(3).
Bloksberg, Leonard N., Connett, Marie B., Rottmann, William H., Forster, Richard L.
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